VALSARTAN
- Product NDC
- 51660-140
- 11-digit product format
- 516600140
- Labeler code
- 51660
- Product ID
- 51660-140_0ea6cbb4-10cd-fecf-e063-6394a90a513b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VALSARTAN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Ohm Laboratories Inc.
- Application
- ANDA077492
- Marketing category
- ANDA
- Marketing start
- 2014-07-07
- 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 |
|---|
| 51660-140-03 | VALSARTAN | 10 in 1 BOTTLE | TABLET, FILM COATED | 10 | | 10 |
| 51660-140-05 | VALSARTAN | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | | 10 |
| 51660-140-30 | VALSARTAN | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 10 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| VALSARTAN | ACTIVE INGREDIENT | 80M03YXJ7I | VALSARTAN TABLET, FILM COATED [OHM LABORATORIES INC.] | 1 | |
| VALSARTAN | ACTIVE MOIETY | 80M03YXJ7I | VALSARTAN TABLET, FILM COATED [OHM LABORATORIES INC.] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | VALSARTAN TABLET, FILM COATED [OHM LABORATORIES INC.] | 1 | |
| CROSPOVIDONE | INACTIVE INGREDIENT | 68401960MK | VALSARTAN TABLET, FILM COATED [OHM LABORATORIES INC.] | 1 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | VALSARTAN TABLET, FILM COATED [OHM LABORATORIES INC.] | 1 | |
| FERRIC OXIDE YELLOW | INACTIVE INGREDIENT | EX438O2MRT | VALSARTAN TABLET, FILM COATED [OHM LABORATORIES INC.] | 1 | |
| FERROSOFERRIC OXIDE | INACTIVE INGREDIENT | XM0M87F357 | VALSARTAN TABLET, FILM COATED [OHM LABORATORIES INC.] | 1 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | VALSARTAN TABLET, FILM COATED [OHM LABORATORIES INC.] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | VALSARTAN TABLET, FILM COATED [OHM LABORATORIES INC.] | 1 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | VALSARTAN TABLET, FILM COATED [OHM LABORATORIES INC.] | 1 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | VALSARTAN TABLET, FILM COATED [OHM LABORATORIES INC.] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | VALSARTAN TABLET, FILM COATED [OHM LABORATORIES INC.] | 1 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | VALSARTAN TABLET, FILM COATED [OHM LABORATORIES INC.] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | VALSARTAN TABLET, FILM COATED [OHM LABORATORIES INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51660-140 | VALSARTAN TABLET, FILM COATED [OHM LABORATORIES INC.] | 10 | Current NDC, Legacy NDC, 3 package rows | 20240112_ab5e0e5a-5bdf-4cfc-9d18-57ea4d642f65.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 |
|---|
| 51660-140-03 | 51660014003 | 10 TABLET, FILM COATED in 1 BOTTLE (51660-140-03) | 2014-07-07 | 0000-00-00 | No | No | Current |
| 51660-140-05 | 51660014005 | 500 TABLET, FILM COATED in 1 BOTTLE (51660-140-05) | 2014-07-07 | 0000-00-00 | No | No | Current |
| 51660-140-30 | 51660014030 | 30 TABLET, FILM COATED in 1 BOTTLE (51660-140-30) | 2014-07-07 | 0000-00-00 | No | No | Current |