cabergoline
Generic: cabergoline
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
cabergoline
Generic Name
cabergoline
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
cabergoline .5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6596
Product ID
50090-6596_537f4ea0-a35c-4826-ba5f-336c9e274000
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076310
Listing Expiration
2026-12-31
Marketing Start
2022-06-15
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906596
Hyphenated Format
50090-6596
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA076310 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .5 mg/1
Packaging
- 8 TABLET in 1 BOTTLE (50090-6596-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "537f4ea0-a35c-4826-ba5f-336c9e274000", "openfda": {"nui": ["M0007652", "N0000175827"], "unii": ["LL60K9J05T"], "rxcui": ["199703"], "spl_set_id": ["7699d938-3f62-4e13-9b33-3e581310b9f3"], "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 (50090-6596-0)", "package_ndc": "50090-6596-0", "marketing_start_date": "20230818"}], "brand_name": "Cabergoline", "product_id": "50090-6596_537f4ea0-a35c-4826-ba5f-336c9e274000", "dosage_form": "TABLET", "pharm_class": ["Ergolines [CS]", "Ergot Derivative [EPC]"], "product_ndc": "50090-6596", "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": "ANDA076310", "marketing_category": "ANDA", "marketing_start_date": "20220615", "listing_expiration_date": "20261231"}