Solifenacin Succinate
- Product NDC
- 71205-580
- 11-digit product format
- 712050580
- Labeler code
- 71205
- Product ID
- 71205-580_2658be08-1517-4b69-8163-710ce69b74e5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- solifenacin succiate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- 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
- 2023-12-31
- 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 |
|---|
| 71205-580 | SOLIFENACIN SUCCINATE (SOLIFENACIN SUCCIATE) TABLET, FILM COATED [PROFICIENT RX LP] | 2 | Legacy NDC | 20220710_ce76ab6e-1f9d-4330-873b-d1b58a1f62bf.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-580-30 | 71205058030 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-580-30) | 2021-06-25 | 0000-00-00 | No | No | Current |
| 71205-580-60 | 71205058060 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-580-60) | 2021-06-25 | 0000-00-00 | No | No | Current |
| 71205-580-90 | 71205058090 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-580-90) | 2021-06-25 | 0000-00-00 | No | No | Current |