Amiloride Hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Avkare, Inc.. The primary component is Amiloride Hydrochloride.
| Product ID | 42291-122_62d4c259-7915-719c-e053-2a91aa0a35de |
| NDC | 42291-122 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Amiloride Hydrochloride |
| Generic Name | Amiloride Hydrochloride |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2012-03-28 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA079133 |
| Labeler Name | AvKARE, Inc. |
| Substance Name | AMILORIDE HYDROCHLORIDE |
| Active Ingredient Strength | 5 mg/1 |
| Pharm Classes | Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2012-03-28 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA079133 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-03-28 |
| Marketing End Date | 2019-07-31 |
| Ingredient | Strength |
|---|---|
| AMILORIDE HYDROCHLORIDE | 5 mg/1 |
| SPL SET ID: | 135f9cb8-17b6-e99a-57c3-2d992eddb8ef |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 42291-122 | Amiloride Hydrochloride | Amiloride Hydrochloride |
| 42794-005 | Amiloride Hydrochloride | Amiloride Hydrochloride |
| 49884-117 | Amiloride Hydrochloride | Amiloride Hydrochloride |
| 50268-071 | Amiloride Hydrochloride | Amiloride Hydrochloride |
| 57721-671 | amiloride hydrochloride | amiloride hydrochloride |
| 60429-275 | Amiloride Hydrochloride | Amiloride Hydrochloride |
| 63629-2114 | Amiloride Hydrochloride | Amiloride Hydrochloride |
| 64980-151 | Amiloride Hydrochloride | Amiloride Hydrochloride |
| 68151-0162 | Amiloride Hydrochloride | Amiloride Hydrochloride |