NDC 0121-0788

CYPROHEPTADINE

Cyproheptadine

CYPROHEPTADINE is a Oral Syrup in the Human Prescription Drug category. It is labeled and distributed by Pharmaceutical Associates, Inc.. The primary component is Cyproheptadine.

• Product ID: 0121-0788_fc72c9e4-1bc6-4d5c-b4e9-ca85e11dc8ba
• NDC: 0121-0788
• Product Type: Human Prescription Drug
• Proprietary Name: CYPROHEPTADINE
• Generic Name: Cyproheptadine
• Dosage Form: Syrup
• Route of Administration: ORAL
• Marketing Start Date: 2013-07-29
• Marketing Category: ANDA / ANDA
• Application Number: ANDA091295
• Labeler Name: Pharmaceutical Associates, Inc.
• Substance Name: CYPROHEPTADINE
• Active Ingredient Strength: 2 mg/5mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0121-0788-16

473 mL in 1 BOTTLE (0121-0788-16)

• Marketing Start Date: 2013-07-29
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0121-0788-16 [00121078816]

CYPROHEPTADINE SYRUP

• Marketing Category: ANDA
• Application Number: ANDA091295
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2013-07-29
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
CYPROHEPTADINE	2 mg/5mL

OpenFDA Data

• SPL SET ID: e3b94a78-0d41-4618-aca5-b1770f945559
• Manufacturer:
  • Pharmaceutical Associates, Inc.
• UNII:
  • 2YHB6175DO
• RxNorm Concept Unique ID - RxCUI:
  • 866021
• UPC Code:
  • 0301210788161

NDC Crossover Matching brand name "CYPROHEPTADINE" or generic name "Cyproheptadine"

NDC	Brand Name	Generic Name
0121-0788	CYPROHEPTADINE	CYPROHEPTADINE
0121-4788	CYPROHEPTADINE	CYPROHEPTADINE
62135-949	CYPROHEPTADINE	CYPROHEPTADINE HYDROCHLORIDE