NDC 33342-115 – Candesartan
Candesartan Cilexetil 8 mg/1 · Tablet · Oral
Product NDC33342-115
Product details
- Brand name
- Candesartan
- Generic name
- Candesartan
- Labeler
- Macleods Pharmaceuticals Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA203813
- Marketed since
- December 6, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker
Active ingredients
- Candesartan Cilexetil 8 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 33342-115-07 | 30 TABLET in 1 CONTAINER (33342-115-07) | Dec 6, 2016 |
| 33342-115-10 | 90 TABLET in 1 CONTAINER (33342-115-10) | Dec 6, 2016 |
| 33342-115-12 | 10 BLISTER PACK in 1 CARTON (33342-115-12) / 10 TABLET in 1 BLISTER PACK | Dec 6, 2016 |
| 33342-115-51 | 300 TABLET in 1 CONTAINER (33342-115-51) | Dec 6, 2016 |
Recalls mentioning this NDC
- D-0329-2021 Apr 21, 2021 · Class III
Failed Impurities/Degradation Specifications
Other Candesartan products
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- 33342-114 Candesartan Cilexetil 4 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