Valsartan
- Product NDC
- 72819-181
- 11-digit product format
- 728190181
- Labeler code
- 72819
- Product ID
- 72819-181_0037a1a4-d769-2567-e063-6394a90a721c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- valsartan
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Archis Pharma LLC
- Application
- ANDA205347
- Marketing category
- ANDA
- Marketing start
- 2022-09-01
- Substance
- VALSARTAN
- Active strength
- 40 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Valsartan
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| VALSARTAN | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 80M03YXJ7I |
| Rxcui | 349199, 349200, 349201, 349483 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72819-181-03 | Valsartan | 30 in 1 BOTTLE, PLASTIC | TABLET, COATED | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72819-181 | VALSARTAN TABLET, COATED [ARCHIS PHARMA LLC] | 4 | Current NDC, Legacy NDC, 1 package rows | 20230712_00b235b2-a909-4628-b37c-bb02bc5bf7c6.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72819-181-03 | 72819018103 | 30 TABLET, COATED in 1 BOTTLE, PLASTIC (72819-181-03) | 2022-09-01 | 0000-00-00 | No | No | Current |