Valsartan
- Product NDC
- 70934-293
- 11-digit product format
- 709340293
- Labeler code
- 70934
- Product ID
- 70934-293_b7b39ad5-e155-b8fe-e053-2995a90a5279
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valsartan
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA204011
- Marketing category
- ANDA
- Marketing start
- 2019-02-22
- Marketing end
- 0000-00-00
- Substance
- VALSARTAN
- Active strength
- 160 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-293-30 | 70934029330 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-293-30) | 30 tablet | 2019-02-22 | 0000-00-00 | No | No | Current |