Package 50742-118-08
Brand: cabergoline
Generic: cabergolinePackage Facts
Identity
Package NDC
50742-118-08
Digits Only
5074211808
Product NDC
50742-118
Description
8 TABLET in 1 BOTTLE (50742-118-08)
Marketing
Marketing Status
Brand
cabergoline
Generic
cabergoline
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9bcb5111-ddb4-46f6-9318-e4a9d51d9e30", "openfda": {"nui": ["M0007652", "N0000175827"], "upc": ["0350742118083"], "unii": ["LL60K9J05T"], "rxcui": ["199703"], "spl_set_id": ["57cbd81e-fdb9-4060-80ee-6e8581c463a4"], "pharm_class_cs": ["Ergolines [CS]"], "pharm_class_epc": ["Ergot Derivative [EPC]"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "8 TABLET in 1 BOTTLE (50742-118-08)", "package_ndc": "50742-118-08", "marketing_start_date": "20180809"}], "brand_name": "Cabergoline", "product_id": "50742-118_9bcb5111-ddb4-46f6-9318-e4a9d51d9e30", "dosage_form": "TABLET", "pharm_class": ["Ergolines [CS]", "Ergot Derivative [EPC]"], "product_ndc": "50742-118", "generic_name": "Cabergoline", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cabergoline", "active_ingredients": [{"name": "CABERGOLINE", "strength": ".5 mg/1"}], "application_number": "ANDA204735", "marketing_category": "ANDA", "marketing_start_date": "20180809", "listing_expiration_date": "20261231"}