Amiloride Hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Avpak. The primary component is Amiloride Hydrochloride.
Product ID | 50268-071_64c9f8c6-b96f-7208-e053-2a91aa0ab6fc |
NDC | 50268-071 |
Product Type | Human Prescription Drug |
Proprietary Name | Amiloride Hydrochloride |
Generic Name | Amiloride Hydrochloride |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2013-01-28 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA079133 |
Labeler Name | AvPAK |
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 | 2013-01-28 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA079133 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-09-19 |
Marketing Category | ANDA |
Application Number | ANDA079133 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-01-28 |
Ingredient | Strength |
---|---|
AMILORIDE HYDROCHLORIDE | 5 mg/1 |
SPL SET ID: | 0d1c0095-8dde-ab90-757b-d031b232e622 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
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 |