cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

cyproheptadine hydrochloride 4 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3517
Product ID 70518-3517_3ab01147-5c61-b2bb-e063-6294a90a9c09
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212491
Listing Expiration 2026-12-31
Marketing Start 2022-09-13

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183517
Hyphenated Format 70518-3517

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
  • 30 TABLET in 1 BLISTER PACK (70518-3517-0)
source: ndc

Packages (1)

70518-3517-0 30 TABLET in 1 BLISTER PACK (70518-3517-0)

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": "3ab01147-5c61-b2bb-e063-6294a90a9c09", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["7b3aed50-cc9e-4897-9735-361225e9e5f2"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3517-0)", "package_ndc": "70518-3517-0", "marketing_start_date": "20220913"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "70518-3517_3ab01147-5c61-b2bb-e063-6294a90a9c09", "dosage_form": "TABLET", "product_ndc": "70518-3517", "generic_name": "CYPROHEPTADINE HYDROCHLORIDE", "labeler_name": "REMEDYREPACK INC.", "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": "20220913", "listing_expiration_date": "20261231"}