NDC 60512-6281

GLONOINUM

Glonoinum

GLONOINUM is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Homeolab Usa Inc.. The primary component is Nitroglycerin.

Product ID60512-6281_074cee98-48a2-4938-b3c2-143cb2999336
NDC60512-6281
Product TypeHuman Otc Drug
Proprietary NameGLONOINUM
Generic NameGlonoinum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2013-11-18
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameHOMEOLAB USA INC.
Substance NameNITROGLYCERIN
Active Ingredient Strength6 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 60512-6281-1

80 PELLET in 1 TUBE (60512-6281-1)
Marketing Start Date2013-11-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 60512-6281-1 [60512628101]

GLONOINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-11-18
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
NITROGLYCERIN6 [hp_X]/1

OpenFDA Data

SPL SET ID:ad27a515-036f-4016-8ecd-498fd181ee65
Manufacturer
UNII

NDC Crossover Matching brand name "GLONOINUM" or generic name "Glonoinum"

NDCBrand NameGeneric Name
0220-2279GlonoinumNITROGLYCERIN
0220-2282GlonoinumNITROGLYCERIN
0220-2283GlonoinumNITROGLYCERIN
0220-2286GlonoinumNITROGLYCERIN
0220-2287GlonoinumNITROGLYCERIN
0220-2290GlonoinumNITROGLYCERIN
0220-2291GlonoinumNITROGLYCERIN
0220-2293GlonoinumNITROGLYCERIN
15631-0207GLONOINUMGLONOINUM
15631-0591GLONOINUMGLONOINUM
37662-1647GlonoinumGlonoinum
37662-1648GlonoinumGlonoinum
37662-1649GlonoinumGlonoinum
37662-1650GlonoinumGlonoinum
37662-1651GlonoinumGlonoinum
37662-1652GlonoinumGlonoinum
37662-1653GlonoinumGlonoinum
37662-1654GlonoinumGlonoinum
37662-1655GlonoinumGlonoinum
60512-6281GLONOINUMGLONOINUM
62106-5945GLONOINUMGlyceryl trinitrate
68428-407GlonoinumNITROGLYCERIN
71919-318GlonoinumNITROGLYCERIN
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.