NDC 15631-0557

CEANOTHUS AMERICANUS

Ceanothus Americanus

CEANOTHUS AMERICANUS 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 Ceanothus Americanus Leaf.

Product ID15631-0557_488a76fb-2a5f-4d8f-936d-a67a61afbe5d
NDC15631-0557
Product TypeHuman Otc Drug
Proprietary NameCEANOTHUS AMERICANUS
Generic NameCeanothus Americanus
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 NameCEANOTHUS AMERICANUS LEAF
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0557-6

1000 TABLET in 1 CONTAINER (15631-0557-6)
Marketing Start Date2015-12-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0557-7 [15631055707]

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

NDC 15631-0557-5 [15631055705]

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

NDC 15631-0557-3 [15631055703]

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

NDC 15631-0557-0 [15631055700]

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

NDC 15631-0557-4 [15631055704]

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

NDC 15631-0557-6 [15631055706]

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

NDC 15631-0557-2 [15631055702]

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

NDC 15631-0557-1 [15631055701]

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

Drug Details

Active Ingredients

IngredientStrength
CEANOTHUS AMERICANUS LEAF1 [hp_X]/1

OpenFDA Data

SPL SET ID:0150cba4-a0ba-4fc4-ba38-3943cfebb872
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "CEANOTHUS AMERICANUS" or generic name "Ceanothus Americanus"

    NDCBrand NameGeneric Name
    0220-1231Ceanothus americanusCEANOTHUS AMERICANUS LEAF
    15631-0119CEANOTHUS AMERICANUSCEANOTHUS AMERICANUS
    15631-0557CEANOTHUS AMERICANUSCEANOTHUS AMERICANUS
    37662-0217Ceanothus AmericanusCeanothus Americanus
    37662-0218Ceanothus AmericanusCeanothus Americanus
    37662-0219Ceanothus AmericanusCeanothus Americanus
    37662-0220Ceanothus AmericanusCeanothus Americanus
    37662-0221Ceanothus AmericanusCeanothus Americanus
    37662-0222Ceanothus AmericanusCeanothus Americanus
    37662-0223Ceanothus AmericanusCeanothus Americanus
    37662-0224Ceanothus AmericanusCeanothus Americanus
    68428-296Ceanothus americanusCEANOTHUS AMERICANUS LEAF
    71919-172Ceanothus americanusCEANOTHUS AMERICANUS LEAF

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