Cyproheptadine Hydrochloride

Product NDC

69339-135

11-digit product format

693390135

Labeler code

69339

Product ID

69339-135_2a764fa2-58e3-4e57-8548-49566165a019

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cyproheptadine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Dash Pharmaceuticals LLC

Application

ANDA207783

Marketing category

ANDA

Marketing start

2017-02-21

Marketing end

2020-10-01

Substance

CYPROHEPTADINE HYDROCHLORIDE

Active strength

4 mg/1

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record