Cabergoline
- Product NDC
- 68071-4596
- 11-digit product format
- 680714596
- Labeler code
- 68071
- Product ID
- 68071-4596_77fbccc1-3b62-96b6-e053-2991aa0a19af
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cabergoline
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA076310
- Marketing category
- ANDA
- Marketing start
- 2005-12-29
- Marketing end
- 0000-00-00
- Substance
- CABERGOLINE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Ergolines [CS],Ergot Derivative [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record