solifenacin succinate
- Product NDC
- 48792-7910
- 11-digit product format
- 487927910
- Labeler code
- 48792
- Product ID
- 48792-7910_a3b8c82b-8380-463e-e053-2995a90ae3b8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- solifenacin succinate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sunshine Lake Pharma Co., Ltd.
- Application
- ANDA213346
- Marketing category
- ANDA
- Marketing start
- 2020-04-25
- 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
- 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 |
|---|
| 48792-7910-1 | 48792791001 | 30 TABLET, FILM COATED in 1 BOTTLE (48792-7910-1) | 2020-04-25 | 0000-00-00 | No | No | Current |
| 48792-7910-2 | 48792791002 | 90 TABLET, FILM COATED in 1 BOTTLE (48792-7910-2) | 2020-04-25 | 0000-00-00 | No | No | Current |