NDC 68382-041 – Promethazine Hydrochloride

Promethazine Hydrochloride 25 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC68382-041

Product details

Brand name
Promethazine Hydrochloride
Generic name
Promethazine Hydrochloride
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040596
Marketed since
December 14, 2005
Listing expires
December 31, 2026
Pharmacologic class
Phenothiazine

Active ingredients

Uses, dosage, side effects and warnings for Promethazine Hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
68382-041-01100 TABLET in 1 BOTTLE (68382-041-01)Dec 14, 2005
68382-041-05500 TABLET in 1 BOTTLE (68382-041-05)Dec 14, 2005
68382-041-101000 TABLET in 1 BOTTLE (68382-041-10)Dec 14, 2005

Recalls mentioning this NDC

Other Promethazine Hydrochloride products