Amlodipine and Valsartan
- Product NDC
- 42291-022
- 11-digit product format
- 422910022
- Labeler code
- 42291
- Product ID
- 42291-022_bf65a563-c414-66e7-e053-2a95a90aa6d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- amlodipine and valsartan
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA090011
- Marketing category
- ANDA
- Marketing start
- 2018-09-11
- Marketing end
- 0000-00-00
- Substance
- AMLODIPINE; VALSARTAN
- Active strength
- 10 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]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-022-30 | 42291002230 | 30 TABLET in 1 BOTTLE, PLASTIC (42291-022-30) | 30 tablet | 2018-09-11 | 0000-00-00 | No | No | Current |