Promethazine Hydrochloride

Product NDC

70934-139

11-digit product format

709340139

Labeler code

70934

Product ID

70934-139_9ae15caa-7a4a-e852-e053-2995a90aed0f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Promethazine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Denton Pharma, Inc. DBA Northwind Pharmaceuticals

Application

ANDA083426

Marketing category

ANDA

Marketing start

2018-10-16

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

2020-12-31

Current FDA listing

Historical FDA.report record