NDC 15631-0007

ADRENALINUM

Adrenalinum

ADRENALINUM 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 Epinephrine.

Product ID15631-0007_11f0447e-5f03-452c-ab9f-8455296b4708
NDC15631-0007
Product TypeHuman Otc Drug
Proprietary NameADRENALINUM
Generic NameAdrenalinum
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 NameEPINEPHRINE
Active Ingredient Strength6 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0007-0

100 PELLET in 1 PACKAGE (15631-0007-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0007-2 [15631000702]

ADRENALINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0007-3 [15631000703]

ADRENALINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0007-5 [15631000705]

ADRENALINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0007-4 [15631000704]

ADRENALINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0007-1 [15631000701]

ADRENALINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0007-0 [15631000700]

ADRENALINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

Drug Details

Active Ingredients

IngredientStrength
EPINEPHRINE6 [hp_X]/1

OpenFDA Data

SPL SET ID:f43f20c4-3cb5-4b5c-8355-0d14db0d74e1
Manufacturer
UNII

NDC Crossover Matching brand name "ADRENALINUM" or generic name "Adrenalinum"

NDCBrand NameGeneric Name
0220-0076AdrenalinumEPINEPHRINE
0220-0078AdrenalinumEPINEPHRINE
15631-0007ADRENALINUMADRENALINUM
60512-6157ADRENALINUMADRENALINUM
66096-778AdrenalinumADRENALINUM
68428-180AdrenalinumEPINEPHRINE
71919-014AdrenalinumEPINEPHRINE
43742-0728EpinephrineAdrenalinum
43742-1243EpinephrineAdrenalinum

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