Valsartan
- Product NDC
- 70771-1885
- 11-digit product format
- 707711885
- Labeler code
- 70771
- Product ID
- 70771-1885_a69225f3-d9ea-4ed4-b7ab-225147cad486
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valsartan
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA218991
- Marketing category
- ANDA
- Marketing start
- 2024-08-30
- 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
- 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 | 320 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 |
|---|
| 70771-1885-9 | Valsartan | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70771-1885 | VALSARTAN TABLET, FILM COATED [ZYDUS LIFESCIENCES LIMITED] | 1 | Current NDC, 1 package rows | 20240830_1b60c816-7399-42c3-8b74-4dc9d82873ec.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70771-1885-9 | 70771188509 | 90 TABLET, FILM COATED in 1 BOTTLE (70771-1885-9) | 2024-08-30 | No | No | Historical |