Candesartan cilexetil
- Product NDC
- 63629-2126
- 11-digit product format
- 636292126
- Labeler code
- 63629
- Product ID
- 63629-2126_a8c953a5-a793-42a4-a37c-51ce47e8cd7d
- 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
- 4 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 |
|---|
| 63629-2126 | CANDESARTAN CILEXETIL TABLET [BRYANT RANCH PREPACK] | 104 | Legacy NDC | 20231129_6b4fa8ce-8592-4569-8e24-c383c05fcf4e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2126-1 | 63629212601 | 90 TABLET in 1 BOTTLE (63629-2126-1) | 90 tablet | 2021-03-10 | 0000-00-00 | No | No | Current |