CYPROHEPTADINE

Product NDC

0121-0788

11-digit product format

001210788

Labeler code

0121

Product ID

0121-0788_fc72c9e4-1bc6-4d5c-b4e9-ca85e11dc8ba

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

CYPROHEPTADINE

Dosage form

SYRUP

Route

ORAL

Labeler

Pharmaceutical Associates, Inc.

Application

ANDA091295

Marketing category

ANDA

Marketing start

2013-07-29

Marketing end

0000-00-00

Substance

CYPROHEPTADINE

Active strength

2 mg/5mL

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record