Oxacillin

Product NDC

70655-109

11-digit product format

706550109

Labeler code

70655

Product ID

70655-109_49fafce3-7142-43a7-9b68-ced39d296f4f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxacillin Sodium

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

Renaissance SSA, LLC

Application

ANDA206681

Marketing category

ANDA

Marketing start

2018-06-01

Marketing end

0000-00-00

Substance

OXACILLIN SODIUM

Active strength

2 g/2g

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