NDC 15631-0573

DIGITALIS PURPUREA

Digitalis Purpurea

DIGITALIS PURPUREA 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 Digitalis.

Product ID15631-0573_44ff0c17-dac8-4b0b-b1a4-eff0089c07b5
NDC15631-0573
Product TypeHuman Otc Drug
Proprietary NameDIGITALIS PURPUREA
Generic NameDigitalis Purpurea
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 NameDIGITALIS
Active Ingredient Strength6 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0573-0

1 TABLET in 1 BLISTER PACK (15631-0573-0)
Marketing Start Date2015-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0573-0 [15631057300]

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

NDC 15631-0573-3 [15631057303]

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

NDC 15631-0573-5 [15631057305]

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

NDC 15631-0573-6 [15631057306]

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

NDC 15631-0573-7 [15631057307]

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

NDC 15631-0573-2 [15631057302]

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

NDC 15631-0573-4 [15631057304]

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

NDC 15631-0573-1 [15631057301]

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

Drug Details

Active Ingredients

IngredientStrength
DIGITALIS6 [hp_X]/1

OpenFDA Data

SPL SET ID:84f23160-aadb-4fd4-b7d5-002bd1c2e369
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "DIGITALIS PURPUREA" or generic name "Digitalis Purpurea"

    NDCBrand NameGeneric Name
    0220-1756Digitalis purpureaDIGITALIS
    0220-1757Digitalis purpureaDIGITALIS
    0220-1761Digitalis purpureaDIGITALIS
    0220-1764Digitalis purpureaDIGITALIS
    0220-1767Digitalis purpureaDIGITALIS
    15631-0167DIGITALIS PURPUREADIGITALIS PURPUREA
    15631-0573DIGITALIS PURPUREADIGITALIS PURPUREA
    37662-0816Digitalis PurpureaDigitalis Purpurea
    37662-0817Digitalis PurpureaDigitalis Purpurea
    37662-0818Digitalis PurpureaDigitalis Purpurea
    37662-0819Digitalis PurpureaDigitalis Purpurea
    37662-0820Digitalis PurpureaDigitalis Purpurea
    37662-0821Digitalis PurpureaDigitalis Purpurea
    37662-0822Digitalis PurpureaDigitalis Purpurea
    37662-0823Digitalis PurpureaDigitalis Purpurea
    37662-0824Digitalis PurpureaDigitalis Purpurea
    60512-6643DIGITALIS PURPUREADIGITALIS PURPUREA
    62106-7878DIGITALIS PURPUREAFoxglove
    71919-256Digitalis purpureaDIGITALIS
    69152-1116Digitalis purpurea 200CDigitalis purpurea

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