Package 50090-7642-0

Brand: cabergoline

Generic: cabergoline
NDC Package

Package Facts

Identity

Package NDC 50090-7642-0
Digits Only 5009076420
Product NDC 50090-7642
Product ID 50090-7642_f0d4a3cf-7de2-4959-b8b6-a2753d0deb15
Description

8 TABLET in 1 BOTTLE (50090-7642-0)

Marketing

Marketing Status
Marketed Since 2025-08-26
Brand cabergoline
Generic cabergoline
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f0d4a3cf-7de2-4959-b8b6-a2753d0deb15", "openfda": {"nui": ["M0007652", "N0000175827"], "unii": ["LL60K9J05T"], "rxcui": ["199703"], "spl_set_id": ["9405c116-4a77-4e14-9ab8-25e899595cdf"], "pharm_class_cs": ["Ergolines [CS]"], "pharm_class_epc": ["Ergot Derivative [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "8 TABLET in 1 BOTTLE (50090-7642-0)", "package_ndc": "50090-7642-0", "marketing_start_date": "20250826"}], "brand_name": "Cabergoline", "product_id": "50090-7642_f0d4a3cf-7de2-4959-b8b6-a2753d0deb15", "dosage_form": "TABLET", "pharm_class": ["Ergolines [CS]", "Ergot Derivative [EPC]"], "product_ndc": "50090-7642", "generic_name": "Cabergoline", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cabergoline", "active_ingredients": [{"name": "CABERGOLINE", "strength": ".5 mg/1"}], "application_number": "ANDA218618", "marketing_category": "ANDA", "marketing_start_date": "20241003", "listing_expiration_date": "20261231"}