cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyproheptadine hydrochloride
Generic Name cyproheptadine hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cyproheptadine hydrochloride 4 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5491
Product ID 50090-5491_28b91c2a-e33a-4b09-8636-4c53ea6f1358
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206553
Listing Expiration 2026-12-31
Marketing Start 2017-01-17

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905491
Hyphenated Format 50090-5491

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 ANDA206553 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-5491-1)
source: ndc

Packages (1)

50090-5491-1 30 TABLET in 1 BOTTLE (50090-5491-1)

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": "28b91c2a-e33a-4b09-8636-4c53ea6f1358", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["7e156e5e-e4cc-420b-8f1a-af123eaa9156"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-5491-1)", "package_ndc": "50090-5491-1", "marketing_start_date": "20210316"}], "brand_name": "Cyproheptadine Hydrochloride", "product_id": "50090-5491_28b91c2a-e33a-4b09-8636-4c53ea6f1358", "dosage_form": "TABLET", "product_ndc": "50090-5491", "generic_name": "Cyproheptadine Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyproheptadine Hydrochloride", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA206553", "marketing_category": "ANDA", "marketing_start_date": "20170117", "listing_expiration_date": "20261231"}