cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride

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

Drug Facts

Product Profile

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

cyproheptadine hydrochloride 4 mg/1

Manufacturer
QUAGEN PHARMACEUTICALS LLC

Identifiers & Regulatory

Product NDC 70752-107
Product ID 70752-107_c83adc2f-bfdf-4fa5-b95b-2a190a7fd78f
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 70752107
Hyphenated Format 70752-107

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 ANDA212491 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (70752-107-10)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (70752-107-11)
source: ndc

Packages (2)

70752-107-10 100 TABLET in 1 BOTTLE, PLASTIC (70752-107-10) 70752-107-11 1000 TABLET in 1 BOTTLE, PLASTIC (70752-107-11)

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": "c83adc2f-bfdf-4fa5-b95b-2a190a7fd78f", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["98e71865-83dd-4e29-8308-c56e36731d96"], "manufacturer_name": ["QUAGEN PHARMACEUTICALS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (70752-107-10)", "package_ndc": "70752-107-10", "marketing_start_date": "20210224"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (70752-107-11)", "package_ndc": "70752-107-11", "marketing_start_date": "20210224"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "70752-107_c83adc2f-bfdf-4fa5-b95b-2a190a7fd78f", "dosage_form": "TABLET", "product_ndc": "70752-107", "generic_name": "CYPROHEPTADINE HYDROCHLORIDE", "labeler_name": "QUAGEN PHARMACEUTICALS LLC", "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"}