cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride

Labeler: avpak
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyproheptadine hydrochloride
Generic Name cyproheptadine hydrochloride
Labeler avpak
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cyproheptadine hydrochloride 4 mg/1

Manufacturer
AvPAK

Identifiers & Regulatory

Product NDC 50268-201
Product ID 50268-201_426ac91c-cb7d-1fe3-e063-6394a90a1d4d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040537
Listing Expiration 2026-12-31
Marketing Start 2025-10-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50268201
Hyphenated Format 50268-201

Supplemental Identifiers

RxCUI
866144
UNII
NJ82J0F8QC

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name cyproheptadine hydrochloride (source: ndc)
Generic Name cyproheptadine hydrochloride (source: ndc)
Application Number ANDA040537 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 50 BLISTER PACK in 1 BOX (50268-201-15) / 1 TABLET in 1 BLISTER PACK (50268-201-11)
source: ndc

Packages (1)

50268-201-15 50 BLISTER PACK in 1 BOX (50268-201-15) / 1 TABLET in 1 BLISTER PACK (50268-201-11)

Ingredients (1)

cyproheptadine hydrochloride (4 mg/1)

Linked Drug Pages (1)

Cyproheptadine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "426ac91c-cb7d-1fe3-e063-6394a90a1d4d", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["426acecc-aef4-099c-e063-6294a90a54eb"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-201-15)  / 1 TABLET in 1 BLISTER PACK (50268-201-11)", "package_ndc": "50268-201-15", "marketing_start_date": "20251030"}], "brand_name": "Cyproheptadine Hydrochloride", "product_id": "50268-201_426ac91c-cb7d-1fe3-e063-6394a90a1d4d", "dosage_form": "TABLET", "product_ndc": "50268-201", "generic_name": "Cyproheptadine Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyproheptadine Hydrochloride", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA040537", "marketing_category": "ANDA", "marketing_start_date": "20251030", "listing_expiration_date": "20261231"}