NDC 42794-005

Amiloride Hydrochloride

Amiloride Hydrochloride

Amiloride Hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Sigmapharm Laboratories, Llc. The primary component is Amiloride Hydrochloride Anhydrous.

Product ID42794-005_c4d496f8-b0d3-46a7-e053-2a95a90a7d45
NDC42794-005
Product TypeHuman Prescription Drug
Proprietary NameAmiloride Hydrochloride
Generic NameAmiloride Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2021-06-14
Marketing CategoryANDA /
Application NumberANDA079133
Labeler NameSigmapharm Laboratories, LLC
Substance NameAMILORIDE HYDROCHLORIDE ANHYDROUS
Active Ingredient Strength5 mg/1
Pharm ClassesDecreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 42794-005-02

100 TABLET in 1 BOTTLE (42794-005-02)
Marketing Start Date2021-06-14
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Amiloride Hydrochloride" or generic name "Amiloride Hydrochloride"

NDCBrand NameGeneric Name
42291-122Amiloride HydrochlorideAmiloride Hydrochloride
42794-005Amiloride HydrochlorideAmiloride Hydrochloride
49884-117Amiloride HydrochlorideAmiloride Hydrochloride
50268-071Amiloride HydrochlorideAmiloride Hydrochloride
57721-671amiloride hydrochlorideamiloride hydrochloride
60429-275Amiloride HydrochlorideAmiloride Hydrochloride
63629-2114Amiloride HydrochlorideAmiloride Hydrochloride
64980-151Amiloride HydrochlorideAmiloride Hydrochloride
68151-0162Amiloride HydrochlorideAmiloride Hydrochloride

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.