Candesartan
- Product NDC
- 0904-7034
- 11-digit product format
- 009047034
- Labeler code
- 0904
- Product ID
- 0904-7034_07ac7ec0-c9ef-4d3d-a6c6-9b042e93699c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Candesartan
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA203813
- Marketing category
- ANDA
- Marketing start
- 2016-12-06
- Marketing end
- 0000-00-00
- Substance
- CANDESARTAN CILEXETIL
- Active strength
- 32 mg/1
- Pharmacologic classes
- 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 |
|---|
| 0904-7034-04 | 00904703404 | 30 BLISTER PACK in 1 CARTON (0904-7034-04) > 1 TABLET in 1 BLISTER PACK | 30 blister pack | 2016-12-06 | 0000-00-00 | No | No | Current |