Candesartan cilexetil
- Product NDC
- 49884-658
- 11-digit product format
- 498840658
- Labeler code
- 49884
- Product ID
- 49884-658_17510ed6-8915-41ab-9f20-8572368f2235
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Candesartan cilexetil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Par Pharmaceutical Inc.
- 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 Product Concepts#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49884-658 | CANDESARTAN CILEXETIL TABLET [PAR PHARMACEUTICAL INC.] | 12 | Legacy NDC | 20240406_1c90aa68-cc12-41ef-aebc-2616ae45683a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49884-658-09 | 49884065809 | 90 TABLET in 1 BOTTLE (49884-658-09) | 90 tablet | 2013-05-21 | 0000-00-00 | No | No | Current |