NDC 0143-1140

Belladonna Alkaloids with Phenobarbital

Belladonna Alkaloids With Phenobarbital

Belladonna Alkaloids with Phenobarbital is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by West-ward Pharmaceuticals Corp. The primary component is Hyoscyamine Sulfate; Atropine Sulfate; Scopolamine Hydrobromide; Phenobarbital.

Product ID0143-1140_88a8ad45-3957-45b0-ae70-d0a11ba0aef9
NDC0143-1140
Product TypeHuman Prescription Drug
Proprietary NameBelladonna Alkaloids with Phenobarbital
Generic NameBelladonna Alkaloids With Phenobarbital
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1966-01-01
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameWest-Ward Pharmaceuticals Corp
Substance NameHYOSCYAMINE SULFATE; ATROPINE SULFATE; SCOPOLAMINE HYDROBROMIDE; PHENOBARBITAL
Active Ingredient Strength0 mg/1; mg/1; mg/1; mg/1
Pharm ClassesAnticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA],Anticholinergic [EPC],Cholinergic Antagonists [MoA]
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 0143-1140-01

100 TABLET in 1 BOTTLE, PLASTIC (0143-1140-01)
Marketing Start Date1966-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0143-1140-51 [00143114051]

Belladonna Alkaloids with Phenobarbital TABLET
Marketing CategoryUNAPPROVED DRUG OTHER
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1966-01-01
Marketing End Date2017-07-17

NDC 0143-1140-01 [00143114001]

Belladonna Alkaloids with Phenobarbital TABLET
Marketing CategoryUNAPPROVED DRUG OTHER
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1966-01-01
Marketing End Date2019-07-31

NDC 0143-1140-10 [00143114010]

Belladonna Alkaloids with Phenobarbital TABLET
Marketing CategoryUNAPPROVED DRUG OTHER
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1966-01-01
Marketing End Date2019-07-31

Drug Details

Active Ingredients

IngredientStrength
HYOSCYAMINE SULFATE.1037 mg/1

OpenFDA Data

SPL SET ID:61b2b8aa-3a2c-4980-925d-df7607132920
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1046815
  • UPC Code
  • 0301431140014
  • Pharmacological Class

    • Anticholinergic [EPC]
    • Cholinergic Antagonists [MoA]
    • Cholinergic Muscarinic Antagonist [EPC]
    • Cholinergic Muscarinic Antagonists [MoA]
    • Anticholinergic [EPC]
    • Cholinergic Antagonists [MoA]

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