Valsartan and Hydrochlorothiazide
- Product NDC
- 53002-1784
- 11-digit product format
- 530021784
- Labeler code
- 53002
- Product ID
- 53002-1784_414b08aa-1c75-4afb-aaf4-4116fb7cf319
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valsartan and Hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA078946
- Marketing category
- ANDA
- Marketing start
- 2013-03-21
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE; VALSARTAN
- Active strength
- 13 mg/1; mg/1
- Pharmacologic classes
- Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 0J48LPH2TH | HYDROCHLOROTHIAZIDE | 58-93-5 | HYDROCHLOROTHIAZIDE |
| 80M03YXJ7I | VALSARTAN | 137862-53-4 | VALSARTAN |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53002-1784-3 | 53002178403 | 30 TABLET, FILM COATED in 1 BOTTLE (53002-1784-3) | 2019-06-01 | 0000-00-00 | No | No | Current |
| 53002-1784-9 | 53002178409 | 90 TABLET, FILM COATED in 1 BOTTLE (53002-1784-9) | 2019-06-01 | 0000-00-00 | No | No | Current |