Package 70069-824-08

Brand: cabergoline

Generic: cabergoline
NDC Package

Package Facts

Identity

Package NDC 70069-824-08
Digits Only 7006982408
Product NDC 70069-824
Product ID 70069-824_999ea838-e592-4769-a702-68d934de3e1d
Description

8 TABLET in 1 BOTTLE (70069-824-08)

Marketing

Marketing Status
Marketed Since 2024-10-18
Brand cabergoline
Generic cabergoline
Sample Package No

Linked Drug Pages (1)

CABERGOLINE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "999ea838-e592-4769-a702-68d934de3e1d", "openfda": {"nui": ["M0007652", "N0000175827"], "upc": ["0370069824085"], "unii": ["LL60K9J05T"], "rxcui": ["199703"], "spl_set_id": ["e0fb5556-de2c-4822-9960-0700e2907890"], "pharm_class_cs": ["Ergolines [CS]"], "pharm_class_epc": ["Ergot Derivative [EPC]"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "8 TABLET in 1 BOTTLE (70069-824-08)", "package_ndc": "70069-824-08", "marketing_start_date": "20241018"}], "brand_name": "CABERGOLINE", "product_id": "70069-824_999ea838-e592-4769-a702-68d934de3e1d", "dosage_form": "TABLET", "pharm_class": ["Ergolines [CS]", "Ergot Derivative [EPC]"], "product_ndc": "70069-824", "generic_name": "CABERGOLINE", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CABERGOLINE", "active_ingredients": [{"name": "CABERGOLINE", "strength": ".5 mg/1"}], "application_number": "ANDA218109", "marketing_category": "ANDA", "marketing_start_date": "20241018", "listing_expiration_date": "20261231"}