NDC 71335-0788

Hyoscyamine SL

Hyoscyamine Sulfate

Hyoscyamine SL is a Oral Tablet, Orally Disintegrating in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Hyoscyamine Sulfate.

Product ID71335-0788_2fed6063-09ea-42e2-a667-a0404ee4715e
NDC71335-0788
Product TypeHuman Prescription Drug
Proprietary NameHyoscyamine SL
Generic NameHyoscyamine Sulfate
Dosage FormTablet, Orally Disintegrating
Route of AdministrationORAL
Marketing Start Date2016-04-15
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameBryant Ranch Prepack
Substance NameHYOSCYAMINE SULFATE
Active Ingredient Strength0 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 71335-0788-1

20 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0788-1)
Marketing Start Date2018-04-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0788-3 [71335078803]

Hyoscyamine SL TABLET, ORALLY DISINTEGRATING
Marketing CategoryUnapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-04-24

NDC 71335-0788-2 [71335078802]

Hyoscyamine SL TABLET, ORALLY DISINTEGRATING
Marketing CategoryUnapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-04-24

NDC 71335-0788-9 [71335078809]

Hyoscyamine SL TABLET, ORALLY DISINTEGRATING
Marketing CategoryUnapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-04-15

NDC 71335-0788-4 [71335078804]

Hyoscyamine SL TABLET, ORALLY DISINTEGRATING
Marketing CategoryUnapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-04-24

NDC 71335-0788-1 [71335078801]

Hyoscyamine SL TABLET, ORALLY DISINTEGRATING
Marketing CategoryUnapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-04-24

NDC 71335-0788-6 [71335078806]

Hyoscyamine SL TABLET, ORALLY DISINTEGRATING
Marketing CategoryUnapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-04-24

NDC 71335-0788-5 [71335078805]

Hyoscyamine SL TABLET, ORALLY DISINTEGRATING
Marketing CategoryUnapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-04-24

NDC 71335-0788-8 [71335078808]

Hyoscyamine SL TABLET, ORALLY DISINTEGRATING
Marketing CategoryUnapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-04-15

NDC 71335-0788-7 [71335078807]

Hyoscyamine SL TABLET, ORALLY DISINTEGRATING
Marketing CategoryUnapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-04-15

Drug Details

Active Ingredients

IngredientStrength
HYOSCYAMINE SULFATE.125 mg/1

OpenFDA Data

SPL SET ID:32699ad4-811e-4b6c-a18c-a0bdf9d9161d
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1046982

    • NDC Crossover Matching brand name "Hyoscyamine SL" or generic name "Hyoscyamine Sulfate"

    NDCBrand NameGeneric Name
    71335-0788Hyoscyamine SLHyoscyamine SL
    51525-0113Hyoscyamine SLHyoscyamine SL
    0225-0295ANASPAZHYOSCYAMINE SULFATE
    0485-0082ED-SPAZHYOSCYAMINE SULFATE
    39328-047HyoscyamineHyoscyamine Sulfate
    39328-048HyoscyamineHyoscyamine Sulfate
    21695-442Hyoscyamine SulfateHyoscyamine Sulfate
    21695-926Hyoscyamine SulfateHyoscyamine Sulfate
    43063-321Hyoscyamine SulfateHyoscyamine Sulfate
    43199-011Hyoscyamine SulfateHyoscyamine Sulfate
    43199-012Hyoscyamine SulfateHyoscyamine Sulfate
    42192-338Hyoscyamine Sulfate ODThyoscyamine sulfate
    42192-339Hyoscyamine Sulfate SLhyoscyamine sulfate
    42192-340Hyoscyamine Sulfate TABhyoscyamine sulfate
    17856-0511HyosyneHyoscyamine Sulfate
    17856-0514HyosyneHyoscyamine Sulfate
    0037-9001LevsinHYOSCYAMINE SULFATE
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