NDC 15631-0165

CYCLAMEN EUROPAEUM

Cyclamen Europaeum

CYCLAMEN EUROPAEUM 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 Cyclamen Purpurascens Tuber.

Product ID15631-0165_a10aef11-cff2-538e-e053-2a95a90acc0d
NDC15631-0165
Product TypeHuman Otc Drug
Proprietary NameCYCLAMEN EUROPAEUM
Generic NameCyclamen Europaeum
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 NameCYCLAMEN PURPURASCENS TUBER
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0165-0

100 PELLET in 1 PACKAGE (15631-0165-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0165-5 [15631016505]

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

NDC 15631-0165-0 [15631016500]

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

NDC 15631-0165-4 [15631016504]

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

NDC 15631-0165-3 [15631016503]

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

NDC 15631-0165-1 [15631016501]

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

NDC 15631-0165-2 [15631016502]

CYCLAMEN EUROPAEUM 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
CYCLAMEN PURPURASCENS TUBER3 [hp_X]/1

OpenFDA Data

SPL SET ID:94c6a042-3f9d-4b24-8a40-8cee8f6b75b8
Manufacturer
UNII

NDC Crossover Matching brand name "CYCLAMEN EUROPAEUM" or generic name "Cyclamen Europaeum"

NDCBrand NameGeneric Name
0220-1638Cyclamen europaeumCYCLAMEN PURPURASCENS TUBER
0220-1639Cyclamen europaeumCYCLAMEN PURPURASCENS TUBER
0220-1640Cyclamen europaeumCYCLAMEN PURPURASCENS TUBER
0220-1643Cyclamen europaeumCYCLAMEN PURPURASCENS TUBER
0220-1644Cyclamen europaeumCYCLAMEN PURPURASCENS TUBER
15631-0165CYCLAMEN EUROPAEUMCYCLAMEN EUROPAEUM
60512-6634CYCLAMEN EUROPAEUMCYCLAMEN EUROPAEUM
68428-353Cyclamen europaeumCYCLAMEN PURPURASCENS TUBER
71919-247Cyclamen europaeumCYCLAMEN PURPURASCENS TUBER

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