NDC 59746-362 – valsartan
Valsartan 160 mg/1 · Tablet · Oral
Product NDC59746-362
Product details
- Brand name
- valsartan
- Generic name
- valsartan
- Labeler
- Jubilant Cadista Pharmaceuticals Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA203536
- Marketed since
- January 5, 2015
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin 2 Receptor Blocker
Active ingredients
- Valsartan 160 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 59746-362-03 | 10 BLISTER PACK in 1 CARTON (59746-362-03) / 10 TABLET in 1 BLISTER PACK | Jan 5, 2015 |
| 59746-362-05 | 500 TABLET in 1 BOTTLE (59746-362-05) | Jan 5, 2015 |
| 59746-362-30 | 30 TABLET in 1 BOTTLE (59746-362-30) | Jan 5, 2015 |
| 59746-362-90 | 90 TABLET in 1 BOTTLE (59746-362-90) | Jan 5, 2015 |
Recalls mentioning this NDC
- D-0461-2021 Jun 2, 2021 · Class II
CGMP Deviations: Intermittent exposure to temperature excursion during storage. - D-1104-2018 Aug 29, 2018 · Class III
Incorrect/Undeclared Excipient: There is a potential an incorrect grade of excipient was used during manufacturing. - D-1103-2018 Aug 29, 2018 · Class III
Incorrect/Undeclared Excipient: There is a potential an incorrect grade of excipient was used during manufacturing. - D-1105-2018 Aug 29, 2018 · Class III
Incorrect/Undeclared Excipient: There is a potential an incorrect grade of excipient was used during manufacturing.
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