Amoxicillin

Product NDC

50090-3480

11-digit product format

500903480

Labeler code

50090

Product ID

50090-3480_86315ba7-6043-461a-8f81-3fab7f61853c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

A-S Medication Solutions

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

2019-12-31

Current FDA listing

Historical FDA.report record