cabergoline
Generic: cabergoline
Labeler: teva pharmaceuticals usa, inc.Drug Facts
Product Profile
Brand Name
cabergoline
Generic Name
cabergoline
Labeler
teva pharmaceuticals usa, inc.
Dosage Form
TABLET
Routes
Active Ingredients
cabergoline .5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0093-5420
Product ID
0093-5420_ee38a597-4dd9-4b40-b168-97e919ead1c7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077750
Listing Expiration
2026-12-31
Marketing Start
2007-03-07
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00935420
Hyphenated Format
0093-5420
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
cabergoline (source: ndc)
Generic Name
cabergoline (source: ndc)
Application Number
ANDA077750 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .5 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (0093-5420-88) / 8 TABLET in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ee38a597-4dd9-4b40-b168-97e919ead1c7", "openfda": {"nui": ["M0007652", "N0000175827"], "unii": ["LL60K9J05T"], "rxcui": ["199703"], "spl_set_id": ["74b61e8a-7ae9-4996-85ec-df23c56de16f"], "pharm_class_cs": ["Ergolines [CS]"], "pharm_class_epc": ["Ergot Derivative [EPC]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0093-5420-88) / 8 TABLET in 1 BOTTLE", "package_ndc": "0093-5420-88", "marketing_start_date": "20070307"}], "brand_name": "Cabergoline", "product_id": "0093-5420_ee38a597-4dd9-4b40-b168-97e919ead1c7", "dosage_form": "TABLET", "pharm_class": ["Ergolines [CS]", "Ergot Derivative [EPC]"], "product_ndc": "0093-5420", "generic_name": "Cabergoline", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cabergoline", "active_ingredients": [{"name": "CABERGOLINE", "strength": ".5 mg/1"}], "application_number": "ANDA077750", "marketing_category": "ANDA", "marketing_start_date": "20070307", "listing_expiration_date": "20261231"}