NDC 15631-0207

GLONOINUM

Glonoinum

GLONOINUM is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Nitroglycerin.

Product ID15631-0207_6b80baed-ec3e-4351-a528-17d7220dd3a4
NDC15631-0207
Product TypeHuman Otc Drug
Proprietary NameGLONOINUM
Generic NameGlonoinum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameNITROGLYCERIN
Active Ingredient Strength6 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0207-0

100 PELLET in 1 PACKAGE (15631-0207-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0207-5 [15631020705]

GLONOINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0207-0 [15631020700]

GLONOINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0207-2 [15631020702]

GLONOINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0207-4 [15631020704]

GLONOINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0207-1 [15631020701]

GLONOINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0207-3 [15631020703]

GLONOINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

Drug Details

Active Ingredients

IngredientStrength
NITROGLYCERIN6 [hp_X]/1

OpenFDA Data

SPL SET ID:6997b44a-4caf-4e2f-a930-50eb71945355
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
60512-6281GLONOINUMGLONOINUM
62106-5945GLONOINUMGlyceryl trinitrate
68428-407GlonoinumNITROGLYCERIN
71919-318GlonoinumNITROGLYCERIN

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