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 71335-1107
Product ID 71335-1107_9a366fac-a3ee-4ed0-926a-03f50fe853d5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209172
Listing Expiration 2026-12-31
Marketing Start 2018-04-11

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351107
Hyphenated Format 71335-1107

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 ANDA209172 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-1107-1)
  • 60 TABLET in 1 BOTTLE (71335-1107-2)
  • 28 TABLET in 1 BOTTLE (71335-1107-3)
  • 100 TABLET in 1 BOTTLE (71335-1107-4)
  • 90 TABLET in 1 BOTTLE (71335-1107-5)
source: ndc

Packages (5)

Ingredients (1)

cyproheptadine hydrochloride (4 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9a366fac-a3ee-4ed0-926a-03f50fe853d5", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["ab58d4df-69d4-43ac-ac6c-871fcc6c946d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1107-1)", "package_ndc": "71335-1107-1", "marketing_start_date": "20190221"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1107-2)", "package_ndc": "71335-1107-2", "marketing_start_date": "20190221"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-1107-3)", "package_ndc": "71335-1107-3", "marketing_start_date": "20190221"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1107-4)", "package_ndc": "71335-1107-4", "marketing_start_date": "20190221"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1107-5)", "package_ndc": "71335-1107-5", "marketing_start_date": "20190221"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "71335-1107_9a366fac-a3ee-4ed0-926a-03f50fe853d5", "dosage_form": "TABLET", "product_ndc": "71335-1107", "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": "ANDA209172", "marketing_category": "ANDA", "marketing_start_date": "20180411", "listing_expiration_date": "20261231"}