NDC 43547-461 – candesartan cilexetil and hydrochlorothiazide
Candesartan Cilexetil 32 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet · Oral
Product NDC43547-461
Product details
- Brand name
- candesartan cilexetil and hydrochlorothiazide
- Generic name
- candesartan cilexetil and hydrochlorothiazide
- Labeler
- Solco Healthcare LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA207455
- Marketed since
- November 20, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Thiazide Diuretic
Active ingredients
- Candesartan Cilexetil 32 mg/1
- Hydrochlorothiazide 25 mg/1
Uses, dosage, side effects and warnings for Candesartan Cilexetil and Hydrochlorothiazide →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 43547-461-09 | 90 TABLET in 1 BOTTLE (43547-461-09) | Nov 20, 2017 |
| 43547-461-50 | 500 TABLET in 1 BOTTLE (43547-461-50) | Nov 20, 2017 |
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- 43547-460 Candesartan Cilexetil 32 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Solco Healthcare LLC
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- 70771-1326 Candesartan Cilexetil 32 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Zydus Lifesciences Limited
- 70771-1327 Candesartan Cilexetil 32 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet · Zydus Lifesciences Limited