NDC 70771-1017 – Bosentan
Bosentan 62.5 mg/1 · Tablet · Oral
Product NDC70771-1017
Product details
- Brand name
- Bosentan
- Generic name
- Bosentan
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA207760
- Marketed since
- May 1, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Endothelin Receptor Antagonist
Active ingredients
- Bosentan 62.5 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 70771-1017-1 | 100 TABLET in 1 BOTTLE (70771-1017-1) | May 1, 2019 |
| 70771-1017-4 | 10 BLISTER PACK in 1 CARTON (70771-1017-4) / 10 TABLET in 1 BLISTER PACK (70771-1017-2) | May 1, 2019 |
| 70771-1017-5 | 500 TABLET in 1 BOTTLE (70771-1017-5) | May 1, 2019 |
| 70771-1017-6 | 60 TABLET in 1 BOTTLE (70771-1017-6) | May 1, 2019 |
| 70771-1017-8 | 180 TABLET in 1 BOTTLE (70771-1017-8) | May 1, 2019 |
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- 47335-038 Bosentan 62.5 mg/1 · Tablet, Film Coated · Sun Pharmaceutical Industries, Inc.
- 47335-039 Bosentan 125 mg/1 · Tablet, Film Coated · Sun Pharmaceutical Industries, Inc.
- 70771-1018 Bosentan 125 mg/1 · Tablet · Zydus Lifesciences Limited
- 70771-1908 Bosentan 32 mg/1 · Tablet, For Suspension · Zydus Lifesciences Limited
- 68382-446 Bosentan 62.5 mg/1 · Tablet, Coated · Zydus Pharmaceuticals USA Inc.
- 68382-447 Bosentan 125 mg/1 · Tablet, Coated · Zydus Pharmaceuticals USA Inc.
- 70710-1508 Bosentan 32 mg/1 · Tablet, For Suspension · Zydus Pharmaceuticals USA Inc.