NDC 15631-0145

COCCULUS INDICUS

Cocculus Indicus

COCCULUS INDICUS 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 Anamirta Cocculus Seed.

Product ID15631-0145_a1084b85-f444-da48-e053-2a95a90a6afa
NDC15631-0145
Product TypeHuman Otc Drug
Proprietary NameCOCCULUS INDICUS
Generic NameCocculus Indicus
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 NameANAMIRTA COCCULUS SEED
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0145-0

100 PELLET in 1 PACKAGE (15631-0145-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0145-2 [15631014502]

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

NDC 15631-0145-0 [15631014500]

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

NDC 15631-0145-5 [15631014505]

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

NDC 15631-0145-1 [15631014501]

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

NDC 15631-0145-3 [15631014503]

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

NDC 15631-0145-4 [15631014504]

COCCULUS INDICUS 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
ANAMIRTA COCCULUS SEED3 [hp_X]/1

OpenFDA Data

SPL SET ID:e107b7ac-82ae-4c53-832c-52cf4552d635
Manufacturer
UNII

NDC Crossover Matching brand name "COCCULUS INDICUS" or generic name "Cocculus Indicus"

NDCBrand NameGeneric Name
0220-1411Cocculus indicusANAMIRTA COCCULUS SEED
0220-1412Cocculus indicusANAMIRTA COCCULUS SEED
0220-1415Cocculus indicusANAMIRTA COCCULUS SEED
0220-1416Cocculus indicusANAMIRTA COCCULUS SEED
0220-1419Cocculus indicusANAMIRTA COCCULUS SEED
0220-1420Cocculus indicusANAMIRTA COCCULUS SEED
0220-1423Cocculus indicusANAMIRTA COCCULUS SEED
0220-1424Cocculus indicusANAMIRTA COCCULUS SEED
0220-1435Cocculus indicusANAMIRTA COCCULUS SEED
0220-1436Cocculus indicusANAMIRTA COCCULUS SEED
0220-1458Cocculus indicusANAMIRTA COCCULUS SEED
0360-0138COCCULUS INDICUSCOCCULUS IND.
15631-0145COCCULUS INDICUSCOCCULUS INDICUS
15631-0565COCCULUS INDICUSCOCCULUS INDICUS
37662-0465Cocculus IndicusCocculus Indicus
37662-0466Cocculus IndicusCocculus Indicus
37662-0467Cocculus IndicusCocculus Indicus
37662-0468Cocculus IndicusCocculus Indicus
37662-0469Cocculus IndicusCocculus Indicus
37662-0470Cocculus IndicusCocculus Indicus
37662-0471Cocculus IndicusCocculus Indicus
37662-0472Cocculus IndicusCocculus Indicus
37662-0473Cocculus IndicusCocculus Indicus
60512-6608COCCULUS INDICUSCOCCULUS INDICUS
62106-7728COCCULUS INDICUSFish berry
68428-329Cocculus indicusANAMIRTA COCCULUS SEED
71919-212Cocculus indicusANAMIRTA COCCULUS SEED
76472-4044COCCULUS INDICUSCOCCULUS INDICUS
76472-4076COCCULUS INDICUSCOCCULUS INDICUS

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