cyproheptadine hydrochloride
Generic: cyproheptadine hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
cyproheptadine hydrochloride
Generic Name
cyproheptadine hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
cyproheptadine hydrochloride 4 mg/1
Manufacturer
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
UNII
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
source: ndc
Resolved Composition
Strengths
- 4 mg/1
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)
Packages (5)
Ingredients (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"}