Temazepam

Product NDC

63739-231

11-digit product format

637390231

Labeler code

63739

Product ID

63739-231_3ad73bbb-bb0f-49fe-bb5b-69040a4cff38

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Temazepam

Dosage form

CAPSULE

Route

ORAL

Labeler

McKesson Corporation dba SKY Packaging

Application

ANDA071427

Marketing category

ANDA

Marketing start

1988-01-12

Marketing end

0000-00-00

Substance

TEMAZEPAM

Active strength

15 mg/1

Pharmacologic classes

Benzodiazepine [EPC],Benzodiazepines [CS]

DEA schedule

CIV

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record