Package 71335-2368-5
Brand: cyproheptadine hydrochloride
Generic: cyproheptadine hydrochloridePackage Facts
Identity
Package NDC
71335-2368-5
Digits Only
7133523685
Product NDC
71335-2368
Description
90 TABLET in 1 BOTTLE (71335-2368-5)
Marketing
Marketing Status
Brand
cyproheptadine hydrochloride
Generic
cyproheptadine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e672afab-de82-4aa0-9d12-f1d7d21dc6c7", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["6a5b5a89-82c2-4991-b026-d160d8fa59a3"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2368-1)", "package_ndc": "71335-2368-1", "marketing_start_date": "20240523"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2368-2)", "package_ndc": "71335-2368-2", "marketing_start_date": "20240523"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-2368-3)", "package_ndc": "71335-2368-3", "marketing_start_date": "20240523"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2368-4)", "package_ndc": "71335-2368-4", "marketing_start_date": "20240523"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2368-5)", "package_ndc": "71335-2368-5", "marketing_start_date": "20240523"}], "brand_name": "Cyproheptadine Hydrochloride", "product_id": "71335-2368_e672afab-de82-4aa0-9d12-f1d7d21dc6c7", "dosage_form": "TABLET", "product_ndc": "71335-2368", "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": "ANDA040537", "marketing_category": "ANDA", "marketing_start_date": "20150729", "listing_expiration_date": "20261231"}