PROMETHAZINE HYDROCHLORIDE

Product NDC

50436-4379

11-digit product format

504364379

Labeler code

50436

Product ID

50436-4379_4008c6a9-f18b-4d8e-8af6-592be18d910d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

promethazine hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA040712

Marketing category

ANDA

Marketing start

2006-07-31

Marketing end

0000-00-00

Substance

PROMETHAZINE HYDROCHLORIDE

Active strength

25 mg/1

Pharmacologic classes

Phenothiazine [EPC],Phenothiazines [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record