Solifenacin Succinate
- Product NDC
- 60687-499
- 11-digit product format
- 606870499
- Labeler code
- 60687
- Product ID
- 60687-499_b050afc2-8100-a772-e053-2a95a90af7e2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Solifenacin Succinate
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA205575
- Marketing category
- ANDA
- Marketing start
- 2019-09-27
- Marketing end
- 2021-04-30
- Substance
- SOLIFENACIN SUCCINATE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 60687-499-21 | 60687049921 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-499-21) > 1 TABLET, COATED in 1 BLISTER PACK (60687-499-11) | 30 blister pack | 2019-09-27 | 2021-04-30 | No | No | Current |