Candesartan cilexetil
- Product NDC
- 60687-241
- 11-digit product format
- 606870241
- Labeler code
- 60687
- Product ID
- 60687-241_e64b400e-9db9-7fba-e053-2a95a90a8aac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Candesartan cilexetil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- NDA020838
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2016-09-12
- Marketing end
- 0000-00-00
- Substance
- CANDESARTAN CILEXETIL
- Active strength
- 16 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 Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60687-241 | CANDESARTAN CILEXETIL TABLET [AMERICAN HEALTH PACKAGING] | 10 | Legacy NDC | 20241123_8d9a7eb7-fe06-4fd4-b6f2-1dd88d91838d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-241-25 | 60687024125 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-241-25) > 1 TABLET in 1 BLISTER PACK (60687-241-95) | 30 blister pack | 2016-09-12 | 0000-00-00 | No | No | Current |