Solifenacin Succinate
- Product NDC
- 71205-540
- 11-digit product format
- 712050540
- Labeler code
- 71205
- Product ID
- 71205-540_31fcb983-1e92-4d12-a997-60346b4fff9f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Solifenacin Succinate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA211657
- Marketing category
- ANDA
- Marketing start
- 2019-09-25
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-540 | SOLIFENACIN SUCCINATE TABLET, FILM COATED [PROFICIENT RX LP] | 1 | Legacy NDC | 20210227_31fcb983-1e92-4d12-a997-60346b4fff9f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-540-30 | 71205054030 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-540-30) | 2021-02-25 | 0000-00-00 | No | No | Current |
| 71205-540-60 | 71205054060 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-540-60) | 2021-02-25 | 0000-00-00 | No | No | Current |
| 71205-540-90 | 71205054090 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-540-90) | 2021-02-25 | 0000-00-00 | No | No | Current |