NDC 68462-387 – Solifenacin succinate
Solifenacin Succinate 10 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC68462-387
Product details
- Brand name
- Solifenacin succinate
- Generic name
- Solifenacin succinate
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA209239
- Marketed since
- May 20, 2019
- Listing expires
- December 31, 2027
- Pharmacologic class
- Cholinergic Muscarinic Antagonist
Active ingredients
- Solifenacin Succinate 10 mg/1
Uses, dosage, side effects and warnings for Solifenacin Succinate →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68462-387-14 | 10 BLISTER PACK in 1 CARTON (68462-387-14) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | May 20, 2019 |
| 68462-387-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-387-30) | May 20, 2019 |
| 68462-387-90 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-387-90) | May 20, 2019 |
Recalls mentioning this NDC
- D-0333-2025 Apr 16, 2025 · Class II
CGMP Deviations - D-0317-2025 Apr 16, 2025 · Class II
CGMP Deviations
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