Amoxicillin

Product NDC

68788-0763

11-digit product format

687880763

Labeler code

68788

Product ID

68788-0763_7d6fd0d0-50af-47da-8cd7-733ac194cf4f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin

Dosage form

TABLET, COATED

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA065255

Marketing category

ANDA

Marketing start

2011-05-18

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

2019-12-31

Current FDA listing

Historical FDA.report record