NDC 15631-0678

SALIX NIGRA

Salix Nigra

SALIX NIGRA 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 Salix Nigra Bark.

Product ID15631-0678_1bdd22e3-e2c6-4a17-9670-0a92c0936b83
NDC15631-0678
Product TypeHuman Otc Drug
Proprietary NameSALIX NIGRA
Generic NameSalix Nigra
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 NameSALIX NIGRA BARK
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0678-5

500 TABLET in 1 CONTAINER (15631-0678-5)
Marketing Start Date2015-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0678-4 [15631067804]

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

NDC 15631-0678-3 [15631067803]

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

NDC 15631-0678-2 [15631067802]

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

NDC 15631-0678-6 [15631067806]

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

NDC 15631-0678-7 [15631067807]

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

NDC 15631-0678-5 [15631067805]

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

NDC 15631-0678-1 [15631067801]

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

NDC 15631-0678-0 [15631067800]

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

Drug Details

Active Ingredients

IngredientStrength
SALIX NIGRA BARK1 [hp_X]/1

OpenFDA Data

SPL SET ID:e228f678-43d4-4993-b68f-e3f26c79bed8
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "SALIX NIGRA" or generic name "Salix Nigra"

    NDCBrand NameGeneric Name
    15631-0385SALIX NIGRASALIX NIGRA
    15631-0678SALIX NIGRASALIX NIGRA
    68428-616Salix nigraSALIX NIGRA BARK
    71919-603Salix nigraSALIX NIGRA BARK
    22840-4416Black Willow PollenSalix nigra
    22840-4491Black Willow PollenSalix nigra
    22840-5478Black Willow PollenSalix nigra
    49643-409Black Willow PollenSalix nigra

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