Cabergoline
- Product NDC
- 70518-2379
- 11-digit product format
- 705182379
- Labeler code
- 70518
- Product ID
- 70518-2379_b97ea08c-8a14-f3ac-e053-2a95a90a5e37
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cabergoline
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204735
- Marketing category
- ANDA
- Marketing start
- 2019-10-23
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2379-0 | 70518237900 | 8 POUCH in 1 BOX, UNIT-DOSE (70518-2379-0) > 1 TABLET in 1 POUCH (70518-2379-1) | 8 pouch | 2019-10-23 | 0000-00-00 | No | No | Current |