cyproheptadine hydrochloride
Generic: cyproheptadine hydrochloride
Labeler: golden state medical supply, inc.Drug Facts
Product Profile
Brand Name
cyproheptadine hydrochloride
Generic Name
cyproheptadine hydrochloride
Labeler
golden state medical supply, inc.
Dosage Form
TABLET
Routes
Active Ingredients
cyproheptadine hydrochloride 4 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51407-272
Product ID
51407-272_3bb806b9-3446-4211-e063-6394a90aff66
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205087
Listing Expiration
2026-12-31
Marketing Start
2015-09-23
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51407272
Hyphenated Format
51407-272
Supplemental Identifiers
RxCUI
UNII
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
ANDA205087 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 mg/1
Packaging
- 1000 TABLET in 1 BOTTLE, PLASTIC (51407-272-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3bb806b9-3446-4211-e063-6394a90aff66", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["95c03949-0e9a-e3b5-e053-2995a90a56b6"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (51407-272-10)", "package_ndc": "51407-272-10", "marketing_start_date": "20190822"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "51407-272_3bb806b9-3446-4211-e063-6394a90aff66", "dosage_form": "TABLET", "product_ndc": "51407-272", "generic_name": "CYPROHEPTADINE HYDROCHLORIDE", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYPROHEPTADINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA205087", "marketing_category": "ANDA", "marketing_start_date": "20150923", "listing_expiration_date": "20261231"}