Amoxicillin

Product NDC

50436-9887

11-digit product format

504369887

Labeler code

50436

Product ID

50436-9887_87602381-d0a2-4795-9c66-168e8ebedee4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA065325

Marketing category

ANDA

Marketing start

2006-06-19

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