Amoxicillin

Product NDC

70518-1008

11-digit product format

705181008

Labeler code

70518

Product ID

70518-1008_8fe541f5-8677-c3b5-e053-2995a90abe92

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA065256

Marketing category

ANDA

Marketing start

2018-02-09

Marketing end

0000-00-00

Substance

AMOXICILLIN

Active strength

875 mg/1

Pharmacologic classes

Penicillin-class Antibacterial [EPC],Penicillins [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record