Rifampin Capsules USP, 300mg, 30-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals,...

FDA Recall #D-0437-2024 — Class II — March 21, 2024

Recall #D-0437-2024 Date: March 21, 2024 Classification: Class II Status: Terminated

Product Description

Rifampin Capsules USP, 300mg, 30-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, Manufactured by: Lupin Limited Aurangabad 431 210 India, NDC 6818-0659-06

Reason for Recall

Subpotent Drug

Recalling Firm

Lupin Pharmaceuticals Inc. — Baltimore, MD

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

26,352 bottles

Distribution

Nationwide within the United States

Code Information

Lot #: A201064, Exp. Date March 2024

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated