Oxacillin

Product NDC

70655-103

11-digit product format

706550103

Labeler code

70655

Product ID

70655-103_73b8e134-3c01-4095-8c81-b50a74932e30

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxacillin Sodium

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAVENOUS

Labeler

Renaissance SSA, LLC

Application

ANDA206760

Marketing category

ANDA

Marketing start

2018-08-01

Marketing end

2020-10-15

Substance

OXACILLIN SODIUM

Active strength

10 g/100mL

Pharmacologic classes

Penicillin-class Antibacterial [EPC],Penicillins [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record