Subpart B - Applications

Applications for FDA Approval to Market a New Drug

FDA-2253-Instructions rev 2021

Subpart B - Applications

OMB: 0910-0001

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INSTRUCTIONS FOR COMPLETING FORM FDA 2253 – TRANSMITTAL OF ADVERTISEMENTS
AND PROMOTIONAL LABELING FOR DRUGS AND BIOLOGICS FOR HUMAN USE
(The item numbers below correspond to the numbered boxes on Form FDA 2253)
1. Date Submitted – The date the 2253 Form and accompanying materials are sent to the FDA. Use dropdown calendar or MM/DD/YYYY format.
2. Application Information – Provide the application type (New Drug Application (NDA), Abbreviated New
Drug Application (ANDA), Biologics License Application (BLA), or Premarket Approval Application (PMA))
from the drop-down followed by the application number. For CBER BLAs enter the supplement number, if
known.
Select either single product or multiple products:
• Single product – Each 2253 Form and accompanying submission should pertain to only one application
number. For paper submissions, the completed Form and the attached submission materials should be
prepared in duplicate, and should be separated for ease of handling.
• Multiple products – A multiple product submission is used for cases where promotional materials mention
multiple products such as price lists, formulary lists, multiple product reminder ads, and corporate
communications. A single application number should be listed on the 2253 Form and the other application
numbers should be included on an attached sheet(s) which identifies the other referenced products
including: application type and number, trade name and established name. Labeling for each referenced
product should be included. For non-eCTD and paper submissions, three specimens of the promotional
piece should be filed to a single application with three 2253 Forms and labeling, and three copies of the
attached sheet(s) showing other referenced products as described above.
3. Proprietary Name – Enter the proprietary name of the drug or biological product. The dosage form should
also be included if it is part of the proprietary name or if it distinguishes the product from other dosage forms
with the same trade name.
4

Established Name – The established (generic) name of the drug/biological product. For biological product
submissions, provide “Product Code No.”, if known or used.

5. Package Insert Date and ID Number – The date and identification number of the most current product
labeling (include two copies for paper submissions).
6. Manufacturer Name and License No. – Provide the manufacturer name. Also include the license number for
biological product submissions.
7. Advertising/Promotional Labeling Materials – A detailed listing of all promotional materials submitted on
the 2253 Form. Each material should be individually listed per line. Individual components of Formulary Kits
and Professional and/or Consumer Kits should be listed separately. Add a new row for each advertisement/
promotional labeling material. Consumer and professional pieces should be submitted separately.
7a. Professional or Consumer – Select only one. If the materials are for mixed audiences, select one audience
(professional or consumer) based on the intended primary audience. If the materials will be viewed by both
professionals and consumers, note this in the Comments section (8f).
7b. Material Type – List materials submitted using the FDA Codes listed below (please see next page).

(continued on next page)
FORM FDA 2253 SUPPLEMENT (11/20 – PREVIOUS VERSION OBSOLETE) – FORM INSTRUCTIONS

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PSC Publishing Services (301) 443-6740 EF

FDA CODE

TRANSLATION

Audio . . . . . . . . . . . . . . . . . . Audio Media (e.g. audio formats other than Internet Audio)
Book . . . . . . . . . . . . . . . . . . Book
Carrier . . . . . . . . . . . . . . . . . Reprint Carrier (e.g. a folder or detail piece that houses a reprint)
Carton . . . . . . . . . . . . . . . . . Sample Carton (e.g. a box or container that houses a drug sample)
Catalog . . . . . . . . . . . . . . . . Catalog (e.g. a pamphlet or book containing a systematically arranged list or record
of items or products)
CD-ROM . . . . . . . . . . . . . . .CD ROMS/Programs/Discs (e.g. a CD ROM that is distributed to health care
professionals or consumers that does not fall into one of the other material types)
Corrective Internet . . . . . . . . Corrective Internet (e.g. corrective materials such as websites, Internet audio, or
Internet video related to a Warning letter)
Corrective Letter . . . . . . . . . Corrective Letter (e.g. corrective letter to health care professionals or consumers or
other printed correctives related to a Warning letter)
Corrective Print Ad. . . . . . . . Corrective print advertisement related to a Warning letter
Corrective TV. . . . . . . . . . . . Corrective TV (e.g. corrective television advertisement related to a Warning letter)
Direct Mail . . . . . . . . . . . . . . Direct Mail (e.g. printed non-electronic materials mailed directly to individuals)
Drug Sample . . . . . . . . . . . . Drug Sample (e.g. a small quantity of prescription drug not intended to be sold and
given to prescribers for dissemination to patients)
Electronic Detail Aid. . . . . . . Electronic Detail Aid (e.g. electronic detail aids, sales aids, or applications used by
sales representatives to detail the product)
Exhibit . . . . . . . . . . . . . . . . . Exhibit (e.g. electronic or non-electronic item(s) set out for public display such as
vertical panels)
File Card . . . . . . . . . . . . . . . File Card
Form . . . . . . . . . . . . . . . . . . Form (e.g. form for subsidy or patient support form)
Formulary Economic. . . . . . Formulary Economic (e.g. material containing cost information about a product
provided to a formulary committee)
Formulary Kit. . . . . . . . . . . . Formulary Kit (e.g. packaged set of materials about a product provided to a
formulary committee)
Giveaway. . . . . . . . . . . . . . . Giveaway
House Organ. . . . . . . . . . . . House Organ (e.g. a periodical issued by a company dedicated to presenting news
about the firm, its products, or its personnel)
Kit . . . . . . . . . . . . . . . . . . . . Kit (e.g. a packaged set of related materials such as a sales kit)
Monograph . . . . . . . . . . . . . Product Monograph
PDURS . . . . . . . . . . . . . . . . Prescription Drug Use Related Software
Press Release. . . . . . . . . . . Press Release
Print Ad . . . . . . . . . . . . . . . . Print Advertisement
Promotional Labeling. . . . . . Promotional Labeling (e.g. generally any labeling other than FDA-required
labeling that is devised for promotion of the product such as brochures, booklets,
or price lists. Use this category when materials do not fall into one of the other
material types.)
Radio. . . . . . . . . . . . . . . . . . Radio (e.g. audio broadcast over radio waves, can include the script)
(continued on next page)
FORM FDA 2253 SUPPLEMENT (11/20 – PREVIOUS VERSION OBSOLETE) – FORM INSTRUCTIONS

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FDA CODE

TRANSLATION

Reply Card. . . . . . . . . . . . . . Reply Card
Reprint. . . . . . . . . . . . . . . . . Reprint (e.g. a reproduction of printed material that has previously appeared in print)
Sales Aid . . . . . . . . . . . . . . . Sales Aid (e.g. print sales aid or detail aid)
Slides. . . . . . . . . . . . . . . . . . Slides (e.g. professional or consumer slide presentations including official notes or
mandatory talking points)
Telephone . . . . . . . . . . . . . . Telephone (e.g. script for telephone calls)
Training Materials . . . . . . . . Training Materials (e.g. learning modules, training video/brochure/other piece(s)
provided to health care professionals or patients)
TV . . . . . . . . . . . . . . . . . . . . Television Advertisement
Video . . . . . . . . . . . . . . . . . . Video (e.g. video other than a Video News Release or Internet Video)
Video News Release . . . . . . Video News Release (e.g. video provided to television newsrooms)
www-audio. . . . . . . . . . . . . . Internet Audio (e.g. podcast or audio conference)
www-banner . . . . . . . . . . . . Internet Banner (e.g. a banner that is intended to be embedded into a web page.)
www-ecomm . . . . . . . . . . . . Internet Electronic Communication (e.g. email directed to health care professionals
or consumers)
www-links . . . . . . . . . . . . . . Internet Link (e.g. sponsored links)
www-mobile. . . . . . . . . . . . . Mobile Technology (e.g. smartphone or tablet app/widget, quick response (QR)
codes, mobile websites)
www-soc-med . . . . . . . . . . . Internet Social Media (e.g. social networking, microblog/blog, online community, wiki)
www-video. . . . . . . . . . . . . . Internet Video
www-website . . . . . . . . . . . . Internet Website
7c. Dissemination/Publication Date – The date of the initial dissemination/publication of the promotional
labeling piece or advertisement. Use drop-down calendar or MM/DD/YYYY format.
7d. Material ID Code – The applicant’s identification code or other designation of the specific
promotional material.
7e. Material Description – The applicant’s description of the specific promotional material.
7f. Comments – Include any information that is pertinent to the dissemination method of the materials. Also
include a comment if a piece is meant to be disseminated exclusively with other pieces and indicate the
accompanying pieces.
8. Applicant (or Agent’s) Return Address, including the country.
9 a, b, & c. Telephone Number, FAX Number, and Email Address – The telephone and facsimile numbers and
email address of the responsible official or agent.
10. Typed Name and Title of Responsible Official or Agent – The individual responsible for responding to any
inquires regarding the 2253 submission.
11. Signature of Responsible Official or Agent
12. Date – Date of signature. Use drop-down calendar or MM/DD/YYYY format.
13. Biological products – For CBER products only, draft or final.

FORM FDA 2253 SUPPLEMENT (11/20 – PREVIOUS VERSION OBSOLETE) – FORM INSTRUCTIONS

(continued on next page)
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NOTE:
Forward Form and attachments for drugs and therapeutic biologic products to: Food and Drug
Administration, Center for Drug Evaluation and Research, Office of Prescription Drug Promotion, 5901-B
Ammendale Road, Beltsville, MD 20705
Forward Form and attachments for biologics to: Food and Drug Administration, Center for Biologics
Evaluation and Research, Document Control Center, 10903 New Hampshire Avenue, Building 71, Room G112,
Silver Spring, MD 20993-0002

FORM FDA 2253 SUPPLEMENT (11/20 – PREVIOUS VERSION OBSOLETE) – FORM INSTRUCTIONS

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PSC Publishing Services (301) 443-6740 EF


File Typeapplication/pdf
File TitleFORM FDA 2253 Instructional Supplement
SubjectInstructions for Completing Form FDA 2253 - Transmittal of Advertisements and Promotional Labeling for Drugs and Biologics for H
AuthorFDA
File Modified2020-11-09
File Created2020-11-09

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