NDC 15631-0298

MOSCHUS

Moschus

MOSCHUS 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 Moschus Moschiferus Musk Sac Resin.

Product ID15631-0298_7ccafc2c-9214-4a8e-92ff-156f00ae63b9
NDC15631-0298
Product TypeHuman Otc Drug
Proprietary NameMOSCHUS
Generic NameMoschus
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-10
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameMOSCHUS MOSCHIFERUS MUSK SAC RESIN
Active Ingredient Strength6 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0298-0

100 PELLET in 1 PACKAGE (15631-0298-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0298-3 [15631029803]

MOSCHUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0298-1 [15631029801]

MOSCHUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0298-5 [15631029805]

MOSCHUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0298-0 [15631029800]

MOSCHUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0298-4 [15631029804]

MOSCHUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0298-2 [15631029802]

MOSCHUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

Drug Details

Active Ingredients

IngredientStrength
MOSCHUS MOSCHIFERUS MUSK SAC RESIN6 [hp_X]/1

OpenFDA Data

SPL SET ID:47155966-4710-43ed-89e1-9f74e3013c82
Manufacturer
UNII

NDC Crossover Matching brand name "MOSCHUS" or generic name "Moschus"

NDCBrand NameGeneric Name
15631-0298MOSCHUSMOSCHUS
68428-514MoschusMOSCHUS MOSCHIFERUS MUSK SAC RESIN
71919-469MoschusMOSCHUS MOSCHIFERUS MUSK SAC RESIN

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