NDC 69238-2261 – Vancomycin Hydrochloride

Vancomycin Hydrochloride 250 mg/5mL · Solution · Oral

Human Prescription Drug 1 recall

Product NDC69238-2261

Product details

Brand name
Vancomycin Hydrochloride
Generic name
Vancomycin Hydrochloride
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA215338
Marketed since
June 26, 2023
Listing expires
December 31, 2027
Pharmacologic class
Glycopeptide Antibacterial

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
69238-2261-380 mL in 1 BOTTLE (69238-2261-3)Jun 26, 2023
69238-2261-5300 mL in 1 BOTTLE (69238-2261-5)Jun 26, 2023
69238-2261-7150 mL in 1 BOTTLE (69238-2261-7)Jun 26, 2023

Recalls mentioning this NDC

Other Vancomycin Hydrochloride products