UNASYN

Product NDC

0049-0022

11-digit product format

000490022

Labeler code

0049

Product ID

0049-0022_d137a407-16ac-4b7b-8646-db443e3e565a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ampicillin sodium and sulbactam sodium

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

Roerig

Application

NDA050608

Marketing category

NDA

Marketing start

1991-11-22

Marketing end

0000-00-00

Substance

AMPICILLIN SODI

Active strength

1 g/1; g/1

Pharmacologic classes

Penicillin-clas

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record