NDC 0093-2264 – Amoxicillin

Amoxicillin 875 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 4 recalls

Product NDC0093-2264

Product details

Brand name
Amoxicillin
Generic name
Amoxicillin
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA065056
Marketed since
September 26, 2000
Listing expires
December 31, 2026
Pharmacologic class
Penicillin-class Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Amoxicillin →

Package NDC codes (1)

Package NDCDescriptionSince
0093-2264-01100 TABLET, FILM COATED in 1 BOTTLE (0093-2264-01)Sep 26, 2000

Recalls mentioning this NDC

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