NDC 15631-0167

DIGITALIS PURPUREA

Digitalis Purpurea

DIGITALIS PURPUREA 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 Digitalis.

Product ID15631-0167_a10b2d82-f7b3-bb25-e053-2995a90ad661
NDC15631-0167
Product TypeHuman Otc Drug
Proprietary NameDIGITALIS PURPUREA
Generic NameDigitalis Purpurea
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 NameDIGITALIS
Active Ingredient Strength6 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0167-0

100 PELLET in 1 PACKAGE (15631-0167-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0167-4 [15631016704]

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

NDC 15631-0167-5 [15631016705]

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

NDC 15631-0167-0 [15631016700]

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

NDC 15631-0167-2 [15631016702]

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

NDC 15631-0167-3 [15631016703]

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

NDC 15631-0167-1 [15631016701]

DIGITALIS PURPUREA 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
DIGITALIS6 [hp_X]/1

OpenFDA Data

SPL SET ID:e24e9770-dc63-4714-b6a0-f418e22a8f83
Manufacturer
UNII

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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