Amoxicillin

Product NDC

42254-139

11-digit product format

422540139

Labeler code

42254

Product ID

42254-139_7aef59fd-9baf-48eb-a16b-1b2ceafd3d84

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

Rebel Distributors Corp

Application

ANDA065325

Marketing category

ANDA

Marketing start

2006-06-19

Marketing end

0000-00-00

Substance

AMOXICILLIN

Active strength

200 mg/5mL

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record