NDC 71335-3032 – Candesartan
Candesartan Cilexetil 16 mg/1 · Tablet · Oral
Product NDC71335-3032
Product details
- Brand name
- Candesartan
- Generic name
- Candesartan
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA203813
- Marketed since
- December 6, 2016
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin 2 Receptor Blocker
Active ingredients
- Candesartan Cilexetil 16 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 71335-3032-1 | 30 TABLET in 1 BOTTLE (71335-3032-1) | Feb 5, 2026 |
| 71335-3032-2 | 90 TABLET in 1 BOTTLE (71335-3032-2) | Feb 5, 2026 |
Other Candesartan products
- 33342-114 Candesartan Cilexetil 4 mg/1 · Tablet · Macleods Pharmaceuticals Limited
- 33342-115 Candesartan Cilexetil 8 mg/1 · Tablet · Macleods Pharmaceuticals Limited
- 33342-116 Candesartan Cilexetil 16 mg/1 · Tablet · Macleods Pharmaceuticals Limited
- 33342-117 Candesartan Cilexetil 32 mg/1 · Tablet · Macleods Pharmaceuticals Limited
- 72603-720 Candesartan Cilexetil 16 mg/1 · Tablet · NorthStar RxLLC
- 72603-721 Candesartan Cilexetil 32 mg/1 · Tablet · NorthStar RxLLC