Candesartan cilexetil
- Product NDC
- 63629-2127
- 11-digit product format
- 636292127
- Labeler code
- 63629
- Product ID
- 63629-2127_547347b8-8b79-42ea-9017-ada9fc8e4916
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Candesartan cilexetil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA020838
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2013-05-21
- Marketing end
- 0000-00-00
- Substance
- CANDESARTAN CILEXETIL
- Active strength
- 8 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-2127 | CANDESARTAN CILEXETIL TABLET [BRYANT RANCH PREPACK] | 105 | Legacy NDC | 20240612_2cdfc8ef-8418-4a2f-8cf3-769596fa9ac6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2127-1 | 63629212701 | 90 TABLET in 1 BOTTLE (63629-2127-1) | 90 tablet | 2021-03-10 | 0000-00-00 | No | No | Current |