Solifenacin Succinate
- Product NDC
- 69367-295
- 11-digit product format
- 693670295
- Labeler code
- 69367
- Product ID
- 69367-295_b67b6a69-0ab9-220b-e053-2a95a90ae6ec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- solifenacin succiate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Westminster Pharmaceuticals, LLC
- Application
- ANDA210281
- Marketing category
- ANDA
- Marketing start
- 2020-11-22
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69367-295-09 | 69367029509 | 90 TABLET, FILM COATED in 1 BOTTLE (69367-295-09) | 2020-11-22 | 0000-00-00 | No | No | Current |
| 69367-295-30 | 69367029530 | 30 TABLET, FILM COATED in 1 BOTTLE (69367-295-30) | 2020-11-22 | 0000-00-00 | No | No | Current |