Amoxicillin

Product NDC

68071-4196

11-digit product format

680714196

Labeler code

68071

Product ID

68071-4196_60ca37b0-b7a3-4287-e053-2991aa0af406

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA061931

Marketing category

ANDA

Marketing start

1990-09-30

Marketing end

0000-00-00

Substance

AMOXICILLIN

Active strength

250 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