cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride

Labeler: qpharma inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyproheptadine hydrochloride
Generic Name cyproheptadine hydrochloride
Labeler qpharma inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cyproheptadine hydrochloride 4 mg/1

Manufacturer
QPharma Inc

Identifiers & Regulatory

Product NDC 42708-177
Product ID 42708-177_459ba568-5598-4ba9-e063-6394a90a0680
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 42708177
Hyphenated Format 42708-177

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
  • 21 TABLET in 1 BOTTLE, PLASTIC (42708-177-21)
source: ndc

Packages (1)

42708-177-21 21 TABLET in 1 BOTTLE, PLASTIC (42708-177-21)

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": "459ba568-5598-4ba9-e063-6394a90a0680", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["fc75bd79-63b7-6388-e053-6394a90ac377"], "manufacturer_name": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "21 TABLET in 1 BOTTLE, PLASTIC (42708-177-21)", "package_ndc": "42708-177-21", "marketing_start_date": "20230605"}], "brand_name": "Cyproheptadine Hydrochloride", "product_id": "42708-177_459ba568-5598-4ba9-e063-6394a90a0680", "dosage_form": "TABLET", "product_ndc": "42708-177", "generic_name": "Cyproheptadine Hydrochloride", "labeler_name": "QPharma Inc", "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"}