NDC 15631-0659

PODOPHYLLUM PELTATUM

Podophyllum Peltatum

PODOPHYLLUM PELTATUM is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Podophyllum.

Product ID15631-0659_2c3a7b86-9743-4c54-96b6-dd2acdcdecc0
NDC15631-0659
Product TypeHuman Otc Drug
Proprietary NamePODOPHYLLUM PELTATUM
Generic NamePodophyllum Peltatum
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-27
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NamePODOPHYLLUM
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0659-6

1000 TABLET in 1 CONTAINER (15631-0659-6)
Marketing Start Date2015-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0659-6 [15631065906]

PODOPHYLLUM PELTATUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0659-2 [15631065902]

PODOPHYLLUM PELTATUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0659-0 [15631065900]

PODOPHYLLUM PELTATUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0659-5 [15631065905]

PODOPHYLLUM PELTATUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0659-7 [15631065907]

PODOPHYLLUM PELTATUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0659-3 [15631065903]

PODOPHYLLUM PELTATUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0659-1 [15631065901]

PODOPHYLLUM PELTATUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0659-4 [15631065904]

PODOPHYLLUM PELTATUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
PODOPHYLLUM3 [hp_X]/1

OpenFDA Data

SPL SET ID:749d8617-0d61-4e1e-926d-e8d89e2c8277
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "PODOPHYLLUM PELTATUM" or generic name "Podophyllum Peltatum"

    NDCBrand NameGeneric Name
    0220-4124Podophyllum peltatumPODOPHYLLUM
    0220-4127Podophyllum peltatumPODOPHYLLUM
    0220-4128Podophyllum peltatumPODOPHYLLUM
    0220-4130Podophyllum peltatumPODOPHYLLUM
    0220-4131Podophyllum peltatumPODOPHYLLUM
    0220-4135Podophyllum peltatumPODOPHYLLUM
    0220-4136Podophyllum peltatumPODOPHYLLUM
    0220-4139Podophyllum peltatumPODOPHYLLUM
    0220-4140Podophyllum peltatumPODOPHYLLUM
    15631-0354PODOPHYLLUM PELTATUMPODOPHYLLUM PELTATUM
    15631-0659PODOPHYLLUM PELTATUMPODOPHYLLUM PELTATUM
    37662-2339Podophyllum PeltatumPodophyllum Peltatum
    37662-2340Podophyllum PeltatumPodophyllum Peltatum
    37662-2341Podophyllum PeltatumPodophyllum Peltatum
    37662-2342Podophyllum PeltatumPodophyllum Peltatum
    37662-2343Podophyllum PeltatumPodophyllum Peltatum
    37662-2344Podophyllum PeltatumPodophyllum Peltatum
    37662-2345Podophyllum PeltatumPodophyllum Peltatum
    37662-2346Podophyllum PeltatumPodophyllum Peltatum
    60512-1038PODOPHYLLUM PELTATUMPODOPHYLLUM PELTATUM
    62106-8648PODOPHYLLUM PELTATUMMayapple
    68428-577Podophyllum peltatumPODOPHYLLUM
    71919-551Podophyllum peltatumPODOPHYLLUM
    69152-1026Podophyllum peltatum 200CPodophyllum peltatum

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