NDC 51655-834 – Valsartan
Valsartan 160 mg/1 · Tablet, Film Coated · Oral
Product NDC51655-834
Product details
- Brand name
- Valsartan
- Generic name
- Valsartan
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203311
- Marketed since
- February 7, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin 2 Receptor Blocker
Active ingredients
- Valsartan 160 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 51655-834-52 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-834-52) | Feb 7, 2023 |
Other Valsartan products
- 50090-6348 Valsartan 160 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-6347 Valsartan 80 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-4130 Valsartan 320 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-6346 Valsartan 320 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 60687-623 Valsartan 80 mg/1 · Tablet, Film Coated · American Health Packaging
- 60687-612 Valsartan 40 mg/1 · Tablet, Film Coated · American Health Packaging
- 60687-634 Valsartan 160 mg/1 · Tablet, Film Coated · American Health Packaging
- 67877-418 Valsartan 320 mg/1 · Tablet, Film Coated · Ascend Laboratories, LLC
- 67877-417 Valsartan 160 mg/1 · Tablet, Film Coated · Ascend Laboratories, LLC
- 67877-416 Valsartan 80 mg/1 · Tablet, Film Coated · Ascend Laboratories, LLC
- 67877-415 Valsartan 40 mg/1 · Tablet, Film Coated · Ascend Laboratories, LLC
- 65862-570 Valsartan 40 mg/1 · Tablet, Film Coated · Aurobindo Pharma Limited