solifenacin succinate
- Product NDC
- 72606-009
- 11-digit product format
- 726060009
- Labeler code
- 72606
- Product ID
- 72606-009_7b2b44a1-cccf-4c95-b0a9-648ec5ca8331
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- solifenacin succinate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- CELLTRION USA, INC.
- Application
- ANDA210582
- 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
- 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 |
|---|
| 72606-009-01 | 72606000901 | 30 TABLET, FILM COATED in 1 BOTTLE (72606-009-01) | 2019-05-20 | 0000-00-00 | No | No | Current |
| 72606-009-02 | 72606000902 | 90 TABLET, FILM COATED in 1 BOTTLE (72606-009-02) | 2019-05-20 | 0000-00-00 | No | No | Current |