NDC 31722-747 – Valsartan
Valsartan 160 mg/1 · Tablet, Film Coated · Oral
Product NDC31722-747
Product details
- Brand name
- Valsartan
- Generic name
- Valsartan
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203311
- Marketed since
- January 5, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker
Active ingredients
- Valsartan 160 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 31722-747-05 | 500 TABLET, FILM COATED in 1 BOTTLE (31722-747-05) | Jan 5, 2015 |
| 31722-747-30 | 30 TABLET, FILM COATED in 1 BOTTLE (31722-747-30) | Jan 5, 2015 |
| 31722-747-31 | 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-747-31) | Jan 5, 2015 |
| 31722-747-32 | 100 TABLET, FILM COATED in 1 BLISTER PACK (31722-747-32) | Jan 5, 2015 |
| 31722-747-90 | 90 TABLET, FILM COATED in 1 BOTTLE (31722-747-90) | Jan 5, 2015 |
Recalls mentioning this NDC
- D-1113-2018 Aug 29, 2018 · Class II
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product. - D-1114-2018 Aug 29, 2018 · Class II
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product. - D-1116-2018 Aug 29, 2018 · Class II
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product. - D-1115-2018 Aug 29, 2018 · Class II
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
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