Solifenacin Succinate
- Product NDC
- 63629-8387
- 11-digit product format
- 636298387
- Labeler code
- 63629
- Product ID
- 63629-8387_7f0bdfbf-d918-439d-aa8a-5b7224dfd35b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Solifenacin Succinate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA209333
- Marketing category
- ANDA
- Marketing start
- 2019-05-20
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8387-1 | 63629838701 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-8387-1) | 2020-11-10 | 0000-00-00 | No | No | Current |
| 63629-8387-2 | 63629838702 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-8387-2) | 2022-09-02 | 0000-00-00 | No | No | Current |