NDC 15631-0024

AMBROSIA ARTEMISIAEFOLIA

Ambrosia Artemisiaefolia

AMBROSIA ARTEMISIAEFOLIA 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 Ambrosia Artemisiifolia.

Product ID15631-0024_9e4a9400-5c13-458c-e053-2995a90add95
NDC15631-0024
Product TypeHuman Otc Drug
Proprietary NameAMBROSIA ARTEMISIAEFOLIA
Generic NameAmbrosia Artemisiaefolia
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-06
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameAMBROSIA ARTEMISIIFOLIA
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0024-0

100 PELLET in 1 PACKAGE (15631-0024-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0024-3 [15631002403]

AMBROSIA ARTEMISIAEFOLIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

NDC 15631-0024-1 [15631002401]

AMBROSIA ARTEMISIAEFOLIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

NDC 15631-0024-5 [15631002405]

AMBROSIA ARTEMISIAEFOLIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

NDC 15631-0024-0 [15631002400]

AMBROSIA ARTEMISIAEFOLIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

NDC 15631-0024-4 [15631002404]

AMBROSIA ARTEMISIAEFOLIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

NDC 15631-0024-2 [15631002402]

AMBROSIA ARTEMISIAEFOLIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

Drug Details

Active Ingredients

IngredientStrength
AMBROSIA ARTEMISIIFOLIA1 [hp_X]/1

OpenFDA Data

SPL SET ID:3625a904-74cf-4405-9830-584ee3fd1b25
Manufacturer
UNII

NDC Crossover Matching brand name "AMBROSIA ARTEMISIAEFOLIA" or generic name "Ambrosia Artemisiaefolia"

NDCBrand NameGeneric Name
0220-0218Ambrosia artemisiaefoliaAMBROSIA ARTEMISIIFOLIA
0220-0219Ambrosia artemisiaefoliaAMBROSIA ARTEMISIIFOLIA
0220-0225Ambrosia artemisiaefoliaAMBROSIA ARTEMISIIFOLIA
15631-0024AMBROSIA ARTEMISIAEFOLIAAMBROSIA ARTEMISIAEFOLIA
60512-6479AMBROSIA ARTEMISIAEFOLIAAMBROSIA ARTEMISIAEFOLIA
68428-196Ambrosia artemisiaefoliaAMBROSIA ARTEMISIIFOLIA
71919-038Ambrosia artemisiaefoliaAMBROSIA ARTEMISIIFOLIA
76097-003Pollen Guard RagweedAmbrosia Artemisiaefolia

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