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Class II Recall — Risk of Temporary or Reversible Adverse Health Consequences
Verified · FDAClass II — Possible RiskMedications

RIFAMPIN Rifampin Capsules USP 150mg, 30-count bottle, Rx Only, Manufactured for: Lupin Recall 2024

RIFAMPINIssued January 5, 2024

RIFAMPIN Rifampin Capsules USP 150mg, 30-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United States, Manufactured Lupin Limited, Aurangabad 431 210 INDIA, ND — recalled per FDA on 1/5/2024. Reason: Subpotent Drug and Failed Impurities/Degradation Specifications.

Issuing agency
FDA
Issued
Jan 5, 2024
Brand
RIFAMPIN
Distribution
1 states

What to do right now

  1. 1

    Stop using it

    Take it out of rotation. Don't consume, wear, or operate.

  2. 2

    Verify the match

    Compare lot numbers, UPCs, and dates against your product.

  3. 3

    Return or dispose

    Follow the manufacturer's instructions to refund or safely dispose.

Verified source

U.S. Food and Drug Administration

Summary of the official FDA notice issued January 5, 2024. Last synced Apr 27, 2026. View on fda.gov

What's recalled

Rifampin Capsules USP 150mg, 30-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United States, Manufactured Lupin Limited, Aurangabad 431 210 INDIA, NDC 68180-658-06

Undeclared allergen alert

This recall involves undeclared allergens not listed on the label:

lupin

Why it was recalled

Subpotent Drug and Failed Impurities/Degradation Specifications

Affected products & lot numbers
1 lot called out

Affected Lot Numbers

Check your product label — do not use if your lot number appears below.

Lot Number
A200816 exp 1/2024 A201248 exp 3/2024
Where was it sold
1 state

Product was distributed to 32 Wholesale/distributor accounts who further distributed the product to 156 distribution sites.

nationwide
View official FDA notice

View all questions for this recall →

More recalls like this
6 related — by brand, contaminant, and category

Frequently asked questions

Is the RIFAMPIN recall still active?

Yes, this recall is currently active as of January 5, 2024. Do not use or consume the affected product.

What lot numbers are affected?

Affected lot numbers: A200816 exp 1/2024 A201248 exp 3/2024. Check the label on your product.

What should I do if I have the recalled RIFAMPIN?

Do not consume or use this product. Return it to the store for a full refund, or dispose of it safely.