RIFAMPIN Rifampin Capsules USP 300mg, 30-count bottle, Rx Only, Manufactured for: Lupin Recall 2024
Official title: Rifampin Capsules USP 300mg, 30-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United States, Manufactured Lupin Limited, Aurangabad 431 210 INDIA, NDC
Verified source
U.S. Food and Drug Administration
This summary mirrors the official FDA notice issued January 5, 2024. Last synced from FDA: Apr 27, 2026.
Rifampin Capsules USP 300mg, 30-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United States, Manufactured Lupin Limited, Aurangabad 431 210 INDIA, NDC 68180-659-06
What's recalled
Rifampin Capsules USP 300mg, 30-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United States, Manufactured Lupin Limited, Aurangabad 431 210 INDIA, NDC 68180-659-06
Undeclared Allergen Alert
This recall involves undeclared allergens not listed on the label:
Affected Lot Numbers
Check your product label — do not use if your lot number appears below.
| Lot Number |
|---|
| A200817 exp 1/2024 |
Why it was recalled
Subpotent Drug and Failed Impurities/Degradation Specifications
Where was it sold
Product was distributed to 32 Wholesale/distributor accounts who further distributed the product to 156 distribution sites.
What to do
- Do not consume or use this product
- Check the lot numbers or UPC codes listed above
- Return the product to the store where you purchased it for a full refund
- Contact your healthcare provider if you have experienced any symptoms
Common questions about this recall →
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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: A200817 exp 1/2024. 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.
Why was RIFAMPIN recalled in 2024?
Subpotent Drug and Failed Impurities/Degradation Specifications