cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyproheptadine hydrochloride
Generic Name cyproheptadine hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cyproheptadine hydrochloride 4 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2964
Product ID 71335-2964_ccf448d1-4daf-4db0-9134-6ea5bf0409eb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212491
Listing Expiration 2026-12-31
Marketing Start 2021-02-24

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352964
Hyphenated Format 71335-2964

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 ANDA212491 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (71335-2964-1)
source: ndc

Packages (1)

71335-2964-1 90 TABLET in 1 BOTTLE (71335-2964-1)

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": "ccf448d1-4daf-4db0-9134-6ea5bf0409eb", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["22eaef18-b5cc-421a-910e-d569f00b4599"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2964-1)", "package_ndc": "71335-2964-1", "marketing_start_date": "20251110"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "71335-2964_ccf448d1-4daf-4db0-9134-6ea5bf0409eb", "dosage_form": "TABLET", "product_ndc": "71335-2964", "generic_name": "CYPROHEPTADINE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYPROHEPTADINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA212491", "marketing_category": "ANDA", "marketing_start_date": "20210224", "listing_expiration_date": "20261231"}