NDC 70518-2191 – Amoxicillin

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

Human Prescription Drug

Product NDC70518-2191

Product details

Brand name
Amoxicillin
Generic name
Amoxicillin
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA065256
Marketed since
July 9, 2019
Listing expires
December 31, 2027
Pharmacologic class
Penicillin-class Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Amoxicillin →

Package NDC codes (4)

Package NDCDescriptionSince
70518-2191-130 TABLET, FILM COATED in 1 BLISTER PACK (70518-2191-1)Jul 9, 2019
70518-2191-220 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2191-2)Jul 19, 2019
70518-2191-314 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2191-3)Jul 19, 2019
70518-2191-414 TABLET, FILM COATED in 1 BLISTER PACK (70518-2191-4)Jul 8, 2020

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