VALSARTAN
- Product NDC
- 43353-203
- 11-digit product format
- 433530203
- Labeler code
- 43353
- Product ID
- 43353-203_5d9f8837-554b-4b8e-ada3-7e705d4806d0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VALSARTAN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA077492
- Marketing category
- ANDA
- Marketing start
- 2014-07-07
- Marketing end
- 0000-00-00
- Substance
- VALSARTAN
- Active strength
- 320 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 43353-203-79 | VALSARTAN | 2160 in 1 BOTTLE | TABLET, FILM COATED | 2160 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43353-203 | VALSARTAN TABLET, FILM COATED [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC] | 1 | Legacy NDC, 1 package rows | 20160714_3768e597-46db-43ab-ac89-f7ddcc2423ce.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 43353-203-79 | 43353020379 | 2160 in 1 BOTTLE | Historical |