AMLODIPINE, VALSARTAN, HYDROCHLOROTHIAZIDE
- Product NDC
- 49884-172
- 11-digit product format
- 498840172
- Labeler code
- 49884
- Product ID
- 49884-172_468724f1-bde7-4497-8028-915d44367e99
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- amlodipine besylate valsartan hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA201087
- Marketing category
- ANDA
- Marketing start
- 2015-06-01
- Marketing end
- 2022-05-31
- Substance
- AMLODIPINE BESYLATE; VALSARTAN; HYDROCHLOROTHIAZIDE
- Active strength
- 5 mg/1; mg/1; mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS],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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49884-172-05 | 49884017205 | 500 TABLET, FILM COATED in 1 BOTTLE (49884-172-05) | 2015-06-01 | 0000-00-00 | No | No | Current |
| 49884-172-09 | 49884017209 | 90 TABLET, FILM COATED in 1 BOTTLE (49884-172-09) | 2015-06-01 | 2022-05-31 | No | No | Current |
| 49884-172-11 | 49884017211 | 30 TABLET, FILM COATED in 1 BOTTLE (49884-172-11) | 2015-06-01 | 2022-05-31 | No | No | Current |