Package 70512-860-08

Brand: cabergoline

Generic: cabergoline
NDC Package

Package Facts

Identity

Package NDC 70512-860-08
Digits Only 7051286008
Product NDC 70512-860
Description

8 TABLET in 1 BOTTLE (70512-860-08)

Marketing

Marketing Status
Marketed Since 2023-05-08
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": "45723c3c-bc96-6df6-e063-6294a90a8e1f", "openfda": {"nui": ["M0007652", "N0000175827"], "upc": ["0370512860080"], "unii": ["LL60K9J05T"], "rxcui": ["199703"], "spl_set_id": ["275a6a25-c3c9-4258-a610-0b00752517f7"], "pharm_class_cs": ["Ergolines [CS]"], "pharm_class_epc": ["Ergot Derivative [EPC]"], "manufacturer_name": ["SOLA Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "8 TABLET in 1 BOTTLE (70512-860-08)", "package_ndc": "70512-860-08", "marketing_start_date": "20230508"}], "brand_name": "Cabergoline", "product_id": "70512-860_45723c3c-bc96-6df6-e063-6294a90a8e1f", "dosage_form": "TABLET", "pharm_class": ["Ergolines [CS]", "Ergot Derivative [EPC]"], "product_ndc": "70512-860", "generic_name": "cabergoline", "labeler_name": "SOLA Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cabergoline", "active_ingredients": [{"name": "CABERGOLINE", "strength": ".5 mg/1"}], "application_number": "ANDA076310", "marketing_category": "ANDA", "marketing_start_date": "20230508", "listing_expiration_date": "20261231"}