Package 0115-1757-01
Brand: cyproheptadine hydrochloride
Generic: cyproheptadine hydrochloridePackage Facts
Identity
Package NDC
0115-1757-01
Digits Only
0115175701
Product NDC
0115-1757
Description
100 TABLET in 1 BOTTLE, PLASTIC (0115-1757-01)
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": "a6cccfd7-dc3b-4191-9319-25a5a6c759f0", "openfda": {"upc": ["0301151757011"], "unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["80e13d3f-f4db-4bb4-95d5-5ac1afa70e7e"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0115-1757-01)", "package_ndc": "0115-1757-01", "marketing_start_date": "20150729"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (0115-1757-03)", "package_ndc": "0115-1757-03", "marketing_start_date": "20150729"}], "brand_name": "Cyproheptadine Hydrochloride", "product_id": "0115-1757_a6cccfd7-dc3b-4191-9319-25a5a6c759f0", "dosage_form": "TABLET", "product_ndc": "0115-1757", "generic_name": "Cyproheptadine Hydrochloride", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "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"}