Candesartan
- Product NDC
- 72603-720
- 11-digit product format
- 726030720
- Labeler code
- 72603
- Product ID
- 72603-720_400810c5-9f59-4285-a3f6-fa98bba0c6a0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Candesartan
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NorthStar RxLLC
- Application
- ANDA203813
- Marketing category
- ANDA
- Marketing start
- 2025-01-29
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Candesartan
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CANDESARTAN CILEXETIL | 16 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | R85M2X0D68 |
| Rxcui | 577776, 639537 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72603-720-01 | Candesartan | 90 in 1 CARTON | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72603-720 | CANDESARTAN TABLET [NORTHSTAR RXLLC] | 1 | Current NDC, 1 package rows | 20250130_880f685f-be01-42f4-9e76-ebd1fcfb1f77.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72603-720-01 | 72603072001 | 90 TABLET in 1 CARTON (72603-720-01) | 90 tablet | 2025-01-29 | No | No | Historical |