NDC 15631-0674

SABADILLA

Sabadilla

SABADILLA 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 Schoenocaulon Officinale Seed.

Product ID15631-0674_2012f40e-8a9a-4ed3-b36a-c99b7aae29c0
NDC15631-0674
Product TypeHuman Otc Drug
Proprietary NameSABADILLA
Generic NameSabadilla
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 NameSCHOENOCAULON OFFICINALE SEED
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0674-7

10000 TABLET in 1 CONTAINER (15631-0674-7)
Marketing Start Date2015-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0674-2 [15631067402]

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

NDC 15631-0674-0 [15631067400]

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

NDC 15631-0674-6 [15631067406]

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

NDC 15631-0674-3 [15631067403]

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

NDC 15631-0674-1 [15631067401]

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

NDC 15631-0674-4 [15631067404]

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

NDC 15631-0674-5 [15631067405]

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

NDC 15631-0674-7 [15631067407]

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

Drug Details

Active Ingredients

IngredientStrength
SCHOENOCAULON OFFICINALE SEED1 [hp_X]/1

OpenFDA Data

SPL SET ID:189ae586-47f2-4f35-b813-93c5e55e642a
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "SABADILLA" or generic name "Sabadilla"

    NDCBrand NameGeneric Name
    0220-4492SabadillaSCHOENOCAULON OFFICINALE SEED
    0220-4493SabadillaSCHOENOCAULON OFFICINALE SEED
    0220-4494SabadillaSCHOENOCAULON OFFICINALE SEED
    0220-4495SabadillaSCHOENOCAULON OFFICINALE SEED
    0220-4496SabadillaSCHOENOCAULON OFFICINALE SEED
    0220-4497SabadillaSCHOENOCAULON OFFICINALE SEED
    0220-4498SabadillaSCHOENOCAULON OFFICINALE SEED
    0220-4499SabadillaSCHOENOCAULON OFFICINALE SEED
    0220-4502SabadillaSCHOENOCAULON OFFICINALE SEED
    15631-0380SABADILLASABADILLA
    15631-0674SABADILLASABADILLA
    37662-1215SabadillaSabadilla
    37662-1216SabadillaSabadilla
    37662-1217SabadillaSabadilla
    37662-1218SabadillaSabadilla
    37662-1219SabadillaSabadilla
    37662-1220SabadillaSabadilla
    37662-1221SabadillaSabadilla
    37662-1222SabadillaSabadilla
    62106-8811SABADILLACevadilla
    68428-610SabadillaSCHOENOCAULON OFFICINALE SEED
    71919-596SabadillaSCHOENOCAULON OFFICINALE SEED
    70413-920EVICTSabadilla
    70413-930EVICTSabadilla

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.