NDC 15631-0321

OOPHORINUM

Oophorinum

OOPHORINUM 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 Sus Scrofa Ovary.

Product ID15631-0321_75736e7d-7e3d-49f1-b88f-4ded7440779d
NDC15631-0321
Product TypeHuman Otc Drug
Proprietary NameOOPHORINUM
Generic NameOophorinum
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 NameSUS SCROFA OVARY
Active Ingredient Strength6 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0321-0

100 PELLET in 1 PACKAGE (15631-0321-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0321-5 [15631032105]

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

NDC 15631-0321-0 [15631032100]

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

NDC 15631-0321-4 [15631032104]

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

NDC 15631-0321-2 [15631032102]

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

NDC 15631-0321-1 [15631032101]

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

NDC 15631-0321-3 [15631032103]

OOPHORINUM 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
SUS SCROFA OVARY6 [hp_X]/1

OpenFDA Data

SPL SET ID:501cbb29-463b-49b5-a24e-0e40b581050b
Manufacturer
UNII

NDC Crossover Matching brand name "OOPHORINUM" or generic name "Oophorinum"

NDCBrand NameGeneric Name
15631-0321OOPHORINUMOOPHORINUM
62106-0286OOPHORINUMOryctolagus cuniculus (Rabbit) Ovary
62106-7109OOPHORINUMOvary
68428-543OophorinumSUS SCROFA OVARY
71919-506OophorinumSUS SCROFA OVARY

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