NDC 15631-0364

RANUNCULUS BULBOSUS

Ranunculus Bulbosus

RANUNCULUS BULBOSUS 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 Ranunculus Bulbosus.

Product ID15631-0364_7fec3785-2481-44b4-ba85-d533bb9f3746
NDC15631-0364
Product TypeHuman Otc Drug
Proprietary NameRANUNCULUS BULBOSUS
Generic NameRanunculus Bulbosus
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-11-05
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameRANUNCULUS BULBOSUS
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0364-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0364-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0364-2 [15631036402]

RANUNCULUS BULBOSUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0364-5 [15631036405]

RANUNCULUS BULBOSUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0364-0 [15631036400]

RANUNCULUS BULBOSUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0364-1 [15631036401]

RANUNCULUS BULBOSUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0364-4 [15631036404]

RANUNCULUS BULBOSUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0364-3 [15631036403]

RANUNCULUS BULBOSUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

Drug Details

Active Ingredients

IngredientStrength
RANUNCULUS BULBOSUS3 [hp_X]/1

OpenFDA Data

SPL SET ID:c6485d63-83e0-48f9-981e-c79ebefc0f29
Manufacturer
UNII

NDC Crossover Matching brand name "RANUNCULUS BULBOSUS" or generic name "Ranunculus Bulbosus"

NDCBrand NameGeneric Name
0220-4314Ranunculus bulbosusRANUNCULUS BULBOSUS
0220-4317Ranunculus bulbosusRANUNCULUS BULBOSUS
0220-4318Ranunculus bulbosusRANUNCULUS BULBOSUS
0220-4319Ranunculus bulbosusRANUNCULUS BULBOSUS
0220-4322Ranunculus bulbosusRANUNCULUS BULBOSUS
0220-4323Ranunculus bulbosusRANUNCULUS BULBOSUS
15631-0364RANUNCULUS BULBOSUSRANUNCULUS BULBOSUS
37662-1420Ranunculus BulbosusRanunculus Bulbosus
37662-1421Ranunculus BulbosusRanunculus Bulbosus
37662-1422Ranunculus BulbosusRanunculus Bulbosus
37662-1423Ranunculus BulbosusRanunculus Bulbosus
37662-1424Ranunculus BulbosusRanunculus Bulbosus
37662-1425Ranunculus BulbosusRanunculus Bulbosus
37662-1426Ranunculus BulbosusRanunculus Bulbosus
37662-1427Ranunculus BulbosusRanunculus Bulbosus
68428-593Ranunculus BulbosusRANUNCULUS BULBOSUS
71919-572Ranunculus bulbosusRANUNCULUS BULBOSUS
69152-1100Ranunculus bulbosus 30CRanunculus bulbosus

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