cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride

Labeler: ingenus pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyproheptadine hydrochloride
Generic Name cyproheptadine hydrochloride
Labeler ingenus pharmaceuticals llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cyproheptadine hydrochloride 4 mg/1

Manufacturer
Ingenus Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 50742-190
Product ID 50742-190_4357bb59-3551-49fd-8fcf-2d90c801776a
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 50742190
Hyphenated Format 50742-190

Supplemental Identifiers

RxCUI
866144
UNII
NJ82J0F8QC

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (50742-190-01)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (50742-190-10)
source: ndc

Packages (2)

50742-190-01 100 TABLET in 1 BOTTLE, PLASTIC (50742-190-01) 50742-190-10 1000 TABLET in 1 BOTTLE, PLASTIC (50742-190-10)

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": "4357bb59-3551-49fd-8fcf-2d90c801776a", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["56f428c9-8d33-4c91-91d8-1fe194335066"], "manufacturer_name": ["Ingenus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (50742-190-01)", "package_ndc": "50742-190-01", "marketing_start_date": "20150923"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (50742-190-10)", "package_ndc": "50742-190-10", "marketing_start_date": "20150923"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "50742-190_4357bb59-3551-49fd-8fcf-2d90c801776a", "dosage_form": "TABLET", "product_ndc": "50742-190", "generic_name": "CYPROHEPTADINE HYDROCHLORIDE", "labeler_name": "Ingenus Pharmaceuticals LLC", "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"}