NDC 15631-0062

ASTERIAS RUBENS

Asterias Rubens

ASTERIAS RUBENS 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 Asterias Rubens.

Product ID15631-0062_9ec8d5ee-ed87-e916-e053-2995a90a38bd
NDC15631-0062
Product TypeHuman Otc Drug
Proprietary NameASTERIAS RUBENS
Generic NameAsterias Rubens
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-12
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameASTERIAS RUBENS
Active Ingredient Strength2 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0062-0

100 PELLET in 1 PACKAGE (15631-0062-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0062-2 [15631006202]

ASTERIAS RUBENS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0062-4 [15631006204]

ASTERIAS RUBENS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0062-3 [15631006203]

ASTERIAS RUBENS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0062-0 [15631006200]

ASTERIAS RUBENS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0062-1 [15631006201]

ASTERIAS RUBENS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0062-5 [15631006205]

ASTERIAS RUBENS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

Drug Details

Active Ingredients

IngredientStrength
ASTERIAS RUBENS2 [hp_X]/1

OpenFDA Data

SPL SET ID:79bb5cbf-b14d-4ead-84c6-d5a83012ae18
Manufacturer
UNII

NDC Crossover Matching brand name "ASTERIAS RUBENS" or generic name "Asterias Rubens"

NDCBrand NameGeneric Name
0220-0616Asterias rubensASTERIAS RUBENS
0220-0617Asterias rubensASTERIAS RUBENS
15631-0062ASTERIAS RUBENSASTERIAS RUBENS
63545-282Asterias RubensAsterias Rubens
63545-283Asterias RubensAsterias Rubens
63545-284Asterias RubensAsterias Rubens
63545-285Asterias RubensAsterias Rubens
63545-287Asterias RubensAsterias Rubens
63545-288Asterias RubensAsterias Rubens
63545-289Asterias RubensAsterias Rubens
63545-290Asterias RubensAsterias Rubens
63545-291Asterias RubensAsterias Rubens
68428-236Asterias rubensASTERIAS RUBENS
71919-096Asterias rubensASTERIAS RUBENS
64117-112AcneASTERIAS RUBENS

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