Promethazine Hydrochloride

Product NDC

40085-220

11-digit product format

400850220

Labeler code

40085

Product ID

40085-220_13e12eae-1995-48f6-ba89-c1e21c2377b6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Promethazine Hydrochloride

Dosage form

SUPPOSITORY

Route

RECTAL

Labeler

Renaissance Pharma, Inc.

Application

ANDA087165

Marketing category

ANDA

Marketing start

2014-08-01

Marketing end

2019-11-30

Substance

PROMETHAZINE HYDROCHLORIDE

Active strength

50 mg/1

Pharmacologic classes

Phenothiazine [EPC],Phenothiazines [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record