Penicillamine Tablets USP 250 mg, 100-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202 Manufactured by: Lupin Limited, Nagpur-441 108, India, NDC# 70748-153-01
Reported: December 20, 2023 Initiated: November 22, 2023 #D-0148-2024
Product Description
Penicillamine Tablets USP 250 mg, 100-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202 Manufactured by: Lupin Limited, Nagpur-441 108, India, NDC# 70748-153-01
Reason for Recall
Failed Dissolution Specifications
Details
- Recalling Firm
- Lupin Pharmaceuticals Inc.
- Units Affected
- N/A
- Distribution
- Product was distributed to 3 wholesale/distributor accounts.
- Location
- Baltimore, MD
Frequently Asked Questions
What product was recalled? ▼
Penicillamine Tablets USP 250 mg, 100-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202 Manufactured by: Lupin Limited, Nagpur-441 108, India, NDC# 70748-153-01. Recalled by Lupin Pharmaceuticals Inc.. Units affected: N/A.
Why was this product recalled? ▼
Failed Dissolution Specifications
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on December 20, 2023. Severity: Moderate. Recall number: D-0148-2024.
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