NDC 62559-660 – Candesartan Cilexetil and Hydrochlorothiazide
Candesartan Cilexetil 16 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral
Product NDC62559-660
Product details
- Brand name
- Candesartan Cilexetil and Hydrochlorothiazide
- Generic name
- Candesartan Cilexetil and Hydrochlorothiazide
- Labeler
- ANI Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA021093
- Marketed since
- September 26, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Thiazide Diuretic
Active ingredients
- Candesartan Cilexetil 16 mg/1
- Hydrochlorothiazide 12.5 mg/1
Uses, dosage, side effects and warnings for Candesartan Cilexetil and Hydrochlorothiazide →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 62559-660-90 | 90 TABLET in 1 BOTTLE (62559-660-90) | Sep 26, 2018 |
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