Amoxicillin

Product NDC

68071-4189

11-digit product format

680714189

Labeler code

68071

Product ID

68071-4189_605220b0-cd5a-7cb9-e053-2a91aa0ac182

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA065334

Marketing category

ANDA

Marketing start

2006-12-28

Marketing end

0000-00-00

Substance

AMOXICILLIN

Active strength

400 mg/5mL

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