NDC 68462-199 – Telmisartan
Telmisartan 20 mg/1 · Tablet · Oral
Product NDC68462-199
Product details
- Brand name
- Telmisartan
- Generic name
- Telmisartan
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA090032
- Marketed since
- July 7, 2014
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin 2 Receptor Blocker
Active ingredients
- Telmisartan 20 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 68462-199-01 | 100 TABLET in 1 BOTTLE (68462-199-01) | Jul 7, 2014 |
| 68462-199-13 | 3 BLISTER PACK in 1 CARTON (68462-199-13) / 10 TABLET in 1 BLISTER PACK | Jul 7, 2014 |
| 68462-199-30 | 30 TABLET in 1 BOTTLE (68462-199-30) | Dec 14, 2020 |
| 68462-199-90 | 90 TABLET in 1 BOTTLE (68462-199-90) | Mar 7, 2024 |
| 68462-199-96 | 6 BLISTER PACK in 1 CARTON (68462-199-96) / 10 TABLET in 1 BLISTER PACK | Dec 14, 2020 |
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