AMPICILLIN

Product NDC

52584-136

11-digit product format

525840136

Labeler code

52584

Product ID

52584-136_f7a71815-1e1d-4097-84c2-511b9db0f2fc

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ampicillin

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

General Injectables & Vaccines, Inc

Application

ANDA062772

Marketing category

ANDA

Marketing start

2013-03-14

Marketing end

0000-00-00

Substance

AMPICILLIN SODIUM

Active strength

1 g/1

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