NDC 15631-0162

CUPRUM ACETICUM

Cuprum Aceticum

CUPRUM ACETICUM 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 Cupric Acetate.

Product ID15631-0162_9b772ec6-f0b7-469d-a525-0037dacd1a11
NDC15631-0162
Product TypeHuman Otc Drug
Proprietary NameCUPRUM ACETICUM
Generic NameCuprum Aceticum
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 NameCUPRIC ACETATE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0162-0

100 PELLET in 1 PACKAGE (15631-0162-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0162-3 [15631016203]

CUPRUM ACETICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0162-2 [15631016202]

CUPRUM ACETICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0162-5 [15631016205]

CUPRUM ACETICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0162-1 [15631016201]

CUPRUM ACETICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0162-4 [15631016204]

CUPRUM ACETICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0162-0 [15631016200]

CUPRUM ACETICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

Drug Details

Active Ingredients

IngredientStrength
CUPRIC ACETATE3 [hp_X]/1

OpenFDA Data

SPL SET ID:15bd58d6-9278-4332-85ec-f713304498f3
Manufacturer
UNII

NDC Crossover Matching brand name "CUPRUM ACETICUM" or generic name "Cuprum Aceticum"

NDCBrand NameGeneric Name
0220-1601Cuprum aceticumCUPRIC ACETATE
15631-0162CUPRUM ACETICUMCUPRUM ACETICUM
37662-0586Cuprum AceticumCuprum Aceticum
37662-0587Cuprum AceticumCuprum Aceticum
37662-0588Cuprum AceticumCuprum Aceticum
37662-0589Cuprum AceticumCuprum Aceticum
37662-0590Cuprum AceticumCuprum Aceticum
37662-0591Cuprum AceticumCuprum Aceticum
37662-0592Cuprum AceticumCuprum Aceticum
37662-0593Cuprum AceticumCuprum Aceticum
68428-928Cuprum aceticumCUPRIC ACETATE
71919-241Cuprum aceticumCUPRIC ACETATE

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