Oxacillin

Product NDC

0781-9113

11-digit product format

007819113

Labeler code

0781

Product ID

0781-9113_94d079a4-dd4d-40e8-aa05-fb8c53810612

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxacillin

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAVENOUS

Labeler

Sandoz Inc

Application

ANDA061490

Marketing category

ANDA

Marketing start

1991-05-09

Marketing end

0000-00-00

Substance

OXACILLIN SODIUM

Active strength

10 g/100mL

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