NDC 68382-688 – Nifedipine
Nifedipine 30 mg/1 · Tablet, Extended Release · Oral
Product NDC68382-688
Product details
- Brand name
- Nifedipine
- Generic name
- Nifedipine
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210184
- Marketed since
- August 18, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Dihydropyridine Calcium Channel Blocker
Active ingredients
- Nifedipine 30 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 68382-688-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-688-01) | Aug 18, 2018 |
| 68382-688-05 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-688-05) | Aug 18, 2018 |
| 68382-688-10 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-688-10) | Aug 18, 2018 |
| 68382-688-16 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-688-16) | Aug 18, 2018 |
| 68382-688-77 | 10 BLISTER PACK in 1 CARTON (68382-688-77) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Aug 18, 2018 |
| 68382-688-95 | 300 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-688-95) | Aug 18, 2018 |
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