NDC 15631-0529

AURUM MURIATICUM NATRONATUM

Aurum Muriaticum Natronatum

AURUM MURIATICUM NATRONATUM 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 Sodium Tetrachloroaurate.

Product ID15631-0529_f4ed2e0a-960b-4a8a-bbd6-df78bb70e15d
NDC15631-0529
Product TypeHuman Otc Drug
Proprietary NameAURUM MURIATICUM NATRONATUM
Generic NameAurum Muriaticum Natronatum
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 NameSODIUM TETRACHLOROAURATE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0529-3

100 TABLET in 1 CONTAINER (15631-0529-3)
Marketing Start Date2015-12-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0529-7 [15631052907]

AURUM MURIATICUM NATRONATUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0529-1 [15631052901]

AURUM MURIATICUM NATRONATUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0529-4 [15631052904]

AURUM MURIATICUM NATRONATUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0529-5 [15631052905]

AURUM MURIATICUM NATRONATUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0529-0 [15631052900]

AURUM MURIATICUM NATRONATUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0529-2 [15631052902]

AURUM MURIATICUM NATRONATUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0529-6 [15631052906]

AURUM MURIATICUM NATRONATUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0529-3 [15631052903]

AURUM MURIATICUM NATRONATUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
SODIUM TETRACHLOROAURATE3 [hp_X]/1

OpenFDA Data

SPL SET ID:c1235cfc-329b-4914-a7d8-d8b5dd58b410
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "AURUM MURIATICUM NATRONATUM" or generic name "Aurum Muriaticum Natronatum"

    NDCBrand NameGeneric Name
    0220-0648Aurum muriaticum natronatumSODIUM TETRACHLOROAURATE
    0220-0649Aurum muriaticum natronatumSODIUM TETRACHLOROAURATE
    0220-0650Aurum muriaticum natronatumSODIUM TETRACHLOROAURATE
    15631-0067AURUM MURIATICUM NATRONATUMAURUM MURIATICUM NATRONATUM
    15631-0529AURUM MURIATICUM NATRONATUMAURUM MURIATICUM NATRONATUM
    63545-317Aurum Muriaticum NatronatumAurum Muriaticum Natronatum
    63545-318Aurum Muriaticum NatronatumAurum Muriaticum Natronatum
    63545-319Aurum Muriaticum NatronatumAurum Muriaticum Natronatum
    63545-320Aurum Muriaticum NatronatumAurum Muriaticum Natronatum
    63545-321Aurum Muriaticum NatronatumAurum Muriaticum Natronatum
    63545-322Aurum Muriaticum NatronatumAurum Muriaticum Natronatum
    63545-323Aurum Muriaticum NatronatumAurum Muriaticum Natronatum
    63545-324Aurum Muriaticum NatronatumAurum Muriaticum Natronatum
    63545-325Aurum Muriaticum NatronatumAurum Muriaticum Natronatum
    63545-653Aurum muriaticum natronatumAurum muriaticum natronatum
    68428-242Aurum muriaticum natronatumSODIUM TETRACHLOROAURATE
    71919-103Aurum muriaticum natronatumSODIUM TETRACHLOROAURATE

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