Telmisartan 68462-0199
Product NDC
68462-0199- Manufacturer
- Glenmark Pharmaceuticals Inc., Usa
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 7, 2014
- Listing Expires
- December 31, 2027
- Application
- ANDA090032
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Telmisartan | 20 mg/1 |
Drug Class
Angiotensin 2 Receptor Blocker [EPC]Angiotensin 2 Receptor Antagonists [MoA]Angiotensin 2 Receptor Blocker [EPC]
Packaging Options(5)
100 TABLET in 1 BOTTLE (68462-199-01)
3 BLISTER PACK in 1 CARTON (68462-199-13) / 10 TABLET in 1 BLISTER PACK
30 TABLET in 1 BOTTLE (68462-199-30)
90 TABLET in 1 BOTTLE (68462-199-90)
6 BLISTER PACK in 1 CARTON (68462-199-96) / 10 TABLET in 1 BLISTER PACK