cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride

Labeler: trupharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyproheptadine hydrochloride
Generic Name cyproheptadine hydrochloride
Labeler trupharma, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cyproheptadine hydrochloride 4 mg/1

Manufacturer
TRUPHARMA, LLC

Identifiers & Regulatory

Product NDC 52817-210
Product ID 52817-210_c67264ab-9491-4aee-a28a-c97e1497915b
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 52817210
Hyphenated Format 52817-210

Supplemental Identifiers

RxCUI
866144
UPC
0352817210500 0352817210104
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 ANDA206553 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (52817-210-10)
  • 500 TABLET in 1 BOTTLE, PLASTIC (52817-210-50)
source: ndc

Packages (2)

52817-210-10 100 TABLET in 1 BOTTLE, PLASTIC (52817-210-10) 52817-210-50 500 TABLET in 1 BOTTLE, PLASTIC (52817-210-50)

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": "c67264ab-9491-4aee-a28a-c97e1497915b", "openfda": {"upc": ["0352817210500", "0352817210104"], "unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["9c0b47c0-ecd2-450f-9dcb-c262db92866e"], "manufacturer_name": ["TRUPHARMA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (52817-210-10)", "package_ndc": "52817-210-10", "marketing_start_date": "20170117"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (52817-210-50)", "package_ndc": "52817-210-50", "marketing_start_date": "20170117"}], "brand_name": "Cyproheptadine Hydrochloride", "product_id": "52817-210_c67264ab-9491-4aee-a28a-c97e1497915b", "dosage_form": "TABLET", "product_ndc": "52817-210", "generic_name": "Cyproheptadine Hydrochloride", "labeler_name": "TRUPHARMA, LLC", "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"}