NDC 68382-471 – Telmisartan
Telmisartan 20 mg/1 · Tablet · Oral
Product NDC68382-471
Product details
- Brand name
- Telmisartan
- Generic name
- Telmisartan
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA203325
- Marketed since
- August 27, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker
Active ingredients
- Telmisartan 20 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 68382-471-01 | 100 TABLET in 1 BOTTLE (68382-471-01) | Aug 27, 2014 |
| 68382-471-05 | 500 TABLET in 1 BOTTLE (68382-471-05) | Aug 27, 2014 |
| 68382-471-06 | 30 TABLET in 1 BOTTLE (68382-471-06) | Aug 27, 2014 |
| 68382-471-10 | 1000 TABLET in 1 BOTTLE (68382-471-10) | Aug 27, 2014 |
| 68382-471-16 | 90 TABLET in 1 BOTTLE (68382-471-16) | Aug 27, 2014 |
| 68382-471-78 | 30 BLISTER PACK in 1 CARTON (68382-471-78) / 1 TABLET in 1 BLISTER PACK (68382-471-30) | Aug 27, 2014 |
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