NDC 15631-0082

BLATTA AMERICANA

Blatta Americana

BLATTA AMERICANA 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 Periplaneta Americana.

Product ID15631-0082_30f810ea-f075-4875-8430-f6692f571cfb
NDC15631-0082
Product TypeHuman Otc Drug
Proprietary NameBLATTA AMERICANA
Generic NameBlatta Americana
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 NamePERIPLANETA AMERICANA
Active Ingredient Strength2 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0082-0

100 PELLET in 1 PACKAGE (15631-0082-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0082-5 [15631008205]

BLATTA AMERICANA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0082-0 [15631008200]

BLATTA AMERICANA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0082-1 [15631008201]

BLATTA AMERICANA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0082-4 [15631008204]

BLATTA AMERICANA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0082-3 [15631008203]

BLATTA AMERICANA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0082-2 [15631008202]

BLATTA AMERICANA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

Drug Details

Active Ingredients

IngredientStrength
PERIPLANETA AMERICANA2 [hp_X]/1

OpenFDA Data

SPL SET ID:7ac0ff7f-aa18-4096-a8a2-386472797284
Manufacturer
UNII

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