Amiloride Hydrochloride - Amiloride Hydrochloride
Navigation: NDC > Supplier starting with: A > AVPAK| Field | Value |
|---|---|
| NDC Code: | 50268-071 |
| Proprietary Name: | Amiloride Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Amiloride Hydrochloride |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 28-01-2013 |
| Category Name: | ANDA |
| Application Number: | ANDA079133 |
| Labeler: | AVPAK |
| Substance Name: | AMILORIDE HYDROCHLORIDE |
| Active Numerator Strength: | 5 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC] |
| DEA Schedule: |