Oxazepam

Product NDC

0781-2810

11-digit product format

007812810

Labeler code

0781

Product ID

0781-2810_8e65c660-bed8-401f-873d-9cf598117aeb

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxazepam

Dosage form

CAPSULE

Route

ORAL

Labeler

Sandoz Inc

Application

ANDA071756

Marketing category

ANDA

Marketing start

1988-04-19

Marketing end

2019-08-31

Substance

OXAZEPAM

Active strength

15 mg/1

Pharmacologic classes

Benzodiazepine [EPC],Benzodiazepines [CS]

DEA schedule

CIV

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record