Solifenacin Succinate
- Product NDC
- 51407-228
- 11-digit product format
- 514070228
- Labeler code
- 51407
- Product ID
- 51407-228_bba5c52d-2ed3-33e1-e053-2995a90a2c59
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- solifenacin succinate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA210281
- Marketing category
- ANDA
- Marketing start
- 2019-05-20
- Marketing end
- 0000-00-00
- Substance
- SOLIFENACIN SUCCINATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-228-30 | 51407022830 | 30 TABLET, FILM COATED in 1 BOTTLE (51407-228-30) | 2019-05-22 | 0000-00-00 | No | No | Current |
| 51407-228-90 | 51407022890 | 90 TABLET, FILM COATED in 1 BOTTLE (51407-228-90) | 2019-05-22 | 0000-00-00 | No | No | Current |