SOLIFENACIN SUCCINATE
- Product NDC
- 69844-048
- 11-digit product format
- 698440048
- Labeler code
- 69844
- Product ID
- 69844-048_8b8bc113-cf28-40be-96fd-9d89f67a3219
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SOLIFENACIN SUCCINATE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Graviti Pharmaceuticals Private Limited
- Application
- ANDA211423
- Marketing category
- ANDA
- Marketing start
- 2020-04-06
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69844-048-01 | 69844004801 | 30 TABLET, FILM COATED in 1 BOTTLE (69844-048-01) | 2020-04-06 | 0000-00-00 | No | No | Current |
| 69844-048-02 | 69844004802 | 90 TABLET, FILM COATED in 1 BOTTLE (69844-048-02) | 2020-04-06 | 0000-00-00 | No | No | Current |