NDC 49884-117 – Amiloride Hydrochloride
Amiloride Hydrochloride Anhydrous 5 mg/1 · Tablet · Oral
Product NDC49884-117
Product details
- Brand name
- Amiloride Hydrochloride
- Generic name
- Amiloride Hydrochloride
- Labeler
- Par Health USA, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA070346
- Marketed since
- January 22, 1986
- Listing expires
- December 31, 2027
- Pharmacologic class
- Potassium-sparing Diuretic
Active ingredients
Uses, dosage, side effects and warnings for Amiloride hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 49884-117-01 | 100 TABLET in 1 BOTTLE (49884-117-01) | May 12, 1986 |
| 49884-117-10 | 1000 TABLET in 1 BOTTLE (49884-117-10) | May 12, 1986 |