MEDICAID DRUG REBATE, REMITTANCE ADVICE REPORT

Forms and Documents

Document Name	Status

No forms / supporting documents in this ICR. Check IC Document Collections.

IC Document Collections

IC ID	Document Title	Status
114140	MEDICAID DRUG REBATE, REMITTANCE ADVICE REPORT Form	Migrated

ICR Details

OMB Control No: 0938-0676	ICR Reference No: 199503-0938-004
Status: Historical Active	Previous ICR Reference No:
Agency/Subagency: HHS/CMS	Agency Tracking No:
Title: MEDICAID DRUG REBATE, REMITTANCE ADVICE REPORT
Type of Information Collection: New collection (Request for a new OMB Control Number)	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 04/12/1995
	Date Received in OIRA: 03/10/1995
Terms of Clearance: This information collection is approved through 7-96 under the following conditions: upon resubmission of this collection HCFA will report on the implementation status of this new form; reaction by drug manufacturers, and the overall success in reducing the number of disputes between manufacturers and the States. HCFA will incorporate comments from the NPRM. HCFA will place the OMB number on the first page of the form, along with an estimate of the burden on respondents. In addition, HCFA will add a statement in the instructions notifying manufacturers that if they do not have a dispute with the invoice, they do not have to complete the RAR and may send payment with the invoice alone.

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	07/31/1996	07/31/1996
Responses	1,928	0	0
Time Burden (Hours)	116,896	0	0
Cost Burden (Dollars)	0	0	0

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Abstract: OBRA 1990 REQUIRES DRUG MANUFACTURERS TO ENTER INTO AND HAVE IN EFFECT A REBATE AGREEMENT WITH HCFA FOR STATES TO RECEIVE FUNDING FOR DRUGS DISPENSED TO MEDICAID RECIPIENTS. 42 CFR 447.534 AND 447.536 REQUIRE MANUFACTURERS TO REPORT SPECIFIC DRUG REBATE INFORMATION TO STATES WHEN PAYMENT IS MADE.

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Authorizing Statute(s): None

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:

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Federal Register Notices & Comments

Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 1

IC Title	Form No.	Form Name
MEDICAID DRUG REBATE, REMITTANCE ADVICE REPORT	HCFA-304

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ICR Summary of Burden

	Total Approved	Previously Approved	Change Due to New Statute	Change Due to Agency Discretion	Change Due to Adjustment in Estimate	Change Due to Potential Violation of the PRA
Annual Number of Responses	1,928	0	0	1,928	0	0
Annual Time Burden (Hours)	116,896	0	0	116,896	0	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

Burden increases because of Program Change due to Agency Discretion: Yes

Burden Increase Due to:

Burden decreases because of Program Change due to Agency Discretion: No

Burden Reduction Due to:

Short Statement:

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Annual Cost to Federal Government: $0

Does this IC contain surveys, censuses, or employ statistical methods? No

Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002? No

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? Uncollected

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? Uncollected

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? Uncollected

Is this ICR related to the Pandemic Response? Uncollected

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Common Form ICR:  No

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On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).

The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:

(a) It is necessary for the proper performance of agency functions;

(b) It avoids unnecessary duplication;

(c) It reduces burden on small entities;

(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;

(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;

(f) It indicates the retention periods for recordkeeping requirements;

(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:

(i) Why the information is being collected;

(ii) Use of information;

(iii) Burden estimate;

(iv) Nature of response (voluntary, required for a benefit, or mandatory);

(v) Nature and extent of confidentiality; and

(vi) Need to display currently valid OMB control number;

(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.

(i) It uses effective and efficient statistical survey methodology (if applicable); and

(j) It makes appropriate use of information technology.

If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.

Certification Date: 03/10/1995

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