Valsartan and Hydrochlorothiazide
- Product NDC
- 71205-258
- 11-digit product format
- 712050258
- Labeler code
- 71205
- Product ID
- 71205-258_09764c50-8d91-4c74-8d5f-d48f79ecb01c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valsartan and Hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA203145
- Marketing category
- ANDA
- Marketing start
- 2013-04-19
- Substance
- HYDROCHLOROTHIAZIDE; VALSARTAN
- Active strength
- 12.5; 160 mg/1; mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Valsartan and Hydrochlorothiazide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HYDROCHLOROTHIAZIDE | 12.5 mg/1 |
| VALSARTAN | 160 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0J48LPH2TH, 80M03YXJ7I |
| Rxcui | 200285 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71205-258-30 | Valsartan and Hydrochlorothiazide | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 4 |
| 71205-258-60 | Valsartan and Hydrochlorothiazide | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 4 |
| 71205-258-90 | Valsartan and Hydrochlorothiazide | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-258 | VALSARTAN AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED [PROFICIENT RX LP] | 4 | Current NDC, Legacy NDC, 3 package rows | 20220722_a9098fc6-3d2a-404f-a4cd-2e181ebbd626.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 |
|---|
| 71205-258-30 | 71205025830 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-258-30) | 2019-05-01 | 0000-00-00 | No | No | Current |
| 71205-258-60 | 71205025860 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-258-60) | 2019-05-01 | 0000-00-00 | No | No | Current |
| 71205-258-90 | 71205025890 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-258-90) | 2019-05-01 | 0000-00-00 | No | No | Current |