cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride

Labeler: unichem pharmaceuticals (usa), inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyproheptadine hydrochloride
Generic Name cyproheptadine hydrochloride
Labeler unichem pharmaceuticals (usa), inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cyproheptadine hydrochloride 4 mg/1

Manufacturer
UNICHEM PHARMACEUTICALS (USA), INC.

Identifiers & Regulatory

Product NDC 76385-130
Product ID 76385-130_d68a0f7b-98e1-4d8c-a236-9d701e4e68d5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206676
Listing Expiration 2027-12-31
Marketing Start 2020-03-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76385130
Hyphenated Format 76385-130

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 ANDA206676 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (76385-130-01)
  • 1000 TABLET in 1 BOTTLE (76385-130-10)
source: ndc

Packages (2)

76385-130-01 100 TABLET in 1 BOTTLE (76385-130-01) 76385-130-10 1000 TABLET in 1 BOTTLE (76385-130-10)

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": "d68a0f7b-98e1-4d8c-a236-9d701e4e68d5", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["99fb821a-fe33-4468-9026-9729a8deff08"], "manufacturer_name": ["UNICHEM PHARMACEUTICALS (USA), INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76385-130-01)", "package_ndc": "76385-130-01", "marketing_start_date": "20200301"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (76385-130-10)", "package_ndc": "76385-130-10", "marketing_start_date": "20200301"}], "brand_name": "Cyproheptadine Hydrochloride", "product_id": "76385-130_d68a0f7b-98e1-4d8c-a236-9d701e4e68d5", "dosage_form": "TABLET", "product_ndc": "76385-130", "generic_name": "Cyproheptadine Hydrochloride", "labeler_name": "UNICHEM PHARMACEUTICALS (USA), INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyproheptadine Hydrochloride", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA206676", "marketing_category": "ANDA", "marketing_start_date": "20200301", "listing_expiration_date": "20271231"}