NDC 15631-0531

AZADIRACHTA INDICA

Azadirachta Indica

AZADIRACHTA INDICA 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 Azadirachta Indica Bark.

Product ID15631-0531_9dc18d3f-bfa5-438b-a061-14b43460f463
NDC15631-0531
Product TypeHuman Otc Drug
Proprietary NameAZADIRACHTA INDICA
Generic NameAzadirachta Indica
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-30
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameAZADIRACHTA INDICA BARK
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0531-2

50 TABLET in 1 CONTAINER (15631-0531-2)
Marketing Start Date2015-12-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0531-0 [15631053100]

AZADIRACHTA INDICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0531-4 [15631053104]

AZADIRACHTA INDICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0531-1 [15631053101]

AZADIRACHTA INDICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0531-7 [15631053107]

AZADIRACHTA INDICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0531-2 [15631053102]

AZADIRACHTA INDICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0531-3 [15631053103]

AZADIRACHTA INDICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0531-5 [15631053105]

AZADIRACHTA INDICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0531-6 [15631053106]

AZADIRACHTA INDICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
AZADIRACHTA INDICA BARK1 [hp_X]/1

OpenFDA Data

SPL SET ID:d47f6ee5-8609-4992-b54c-66417f37da51
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "AZADIRACHTA INDICA" or generic name "Azadirachta Indica"

    NDCBrand NameGeneric Name
    15631-0531AZADIRACHTA INDICAAZADIRACHTA INDICA
    68428-245Azadirachta indicaAZADIRACHTA INDICA BARK
    71919-106Azadirachta indicaAZADIRACHTA INDICA BARK
    76441-909Lice-Nil LICE AND EGGS ELIMINATOR OilAZADIRACHTA INDICA

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