Oxacillin

Product NDC

0781-9109

11-digit product format

007819109

Labeler code

0781

Product ID

0781-9109_caf8e10f-c7c3-485e-b28d-5a7fe723f34e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxacillin

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

Sandoz Inc

Application

ANDA061490

Marketing category

ANDA

Marketing start

1976-01-06

Marketing end

0000-00-00

Substance

OXACILLIN SODIUM

Active strength

1 g/1

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