NDC 70748-153 – Penicillamine

Penicillamine 250 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC70748-153

Product details

Brand name
Penicillamine
Generic name
Penicillamine
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA212933
Marketed since
March 1, 2021
Listing expires
December 31, 2026
Pharmacologic class
Antirheumatic Agent

Active ingredients

Uses, dosage, side effects and warnings for Penicillamine →

Package NDC codes (1)

Package NDCDescriptionSince
70748-153-01100 TABLET in 1 BOTTLE (70748-153-01)Mar 1, 2021

Recalls mentioning this NDC

Other Penicillamine products