NDC 66993-473 – Nisoldipine
Nisoldipine 17 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC66993-473
Product details
- Brand name
- Nisoldipine
- Generic name
- Nisoldipine
- Labeler
- Prasco Laboratories
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA020356
- Marketed since
- February 27, 2012
- Marketing end
- May 31, 2027
- Pharmacologic class
- Dihydropyridine Calcium Channel Blocker
Active ingredients
- Nisoldipine 17 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 66993-473-02 | 1 BOTTLE in 1 CARTON (66993-473-02) / 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE | Feb 27, 2012 |
Recalls mentioning this NDC
- D-1284-2015 Aug 12, 2015 · Class III
Failed Dissolution Specifications
Other Nisoldipine products
- 23155-976 Nisoldipine 8.5 mg/1 · Tablet, Film Coated, Extended Release · Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- 23155-977 Nisoldipine 17 mg/1 · Tablet, Film Coated, Extended Release · Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- 66993-472 Nisoldipine 8.5 mg/1 · Tablet, Film Coated, Extended Release · Prasco Laboratories
- 66993-475 Nisoldipine 34 mg/1 · Tablet, Film Coated, Extended Release · Prasco Laboratories