71554-003 NDC - CYPROHEPTADINE HYDROCHLORIDE

Drug Information

Product NDC: 71554-003
Proprietary Name:
Non Proprietary Name: Cyproheptadine Hydrochloride
Active Ingredient(s): 1 kg/kg CYPROHEPTADINE HYDROCHLORIDE
Administration Route(s):
Dosage Form(s): POWDER

Labeler Information

Field Name	Field Value
Labeler Name:	R.L.Fine Chem Private Limited
Product Type:	BULK INGREDIENT
FDA Application Number:
Marketing Category:	BULK INGREDIENT
Start Marketing Date:	4/25/2019

Package Information

No.	Package Code	Package Description	Billing Unit
1	71554-003-01	5 kg in 1 DRUM (71554-003-01)
2	71554-003-02	10 kg in 1 DRUM (71554-003-02)
3	71554-003-03	25 kg in 1 DRUM (71554-003-03)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	71554-003	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Cyproheptadine Hydrochloride	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	4/25/2019	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
LABELER NAME	R.L.Fine Chem Private Limited	This is the date that the labeler indicates was the start of its marketing of the drug product.
SUBSTANCE NAME	CYPROHEPTADINE HYDROCHLORIDE	This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
ACTIVE NUMERATOR STRENGTH	1
ACTIVE INGRED UNIT	kg/kg

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This page was last updated on: 3/6/2026

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