Product NDC: | 63629-4838 |
Proprietary Name: | Hyoscyamine Sulfate |
Non Proprietary Name: | Hyoscyamine Sulfate |
Active Ingredient(s): | .125 mg/1 & nbsp; Hyoscyamine Sulfate |
Administration Route(s): | ORAL; SUBLINGUAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63629-4838 |
Labeler Name: | Bryant Ranch Prepack |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20090921 |
Package NDC: | 63629-4838-1 |
Package Description: | 20 TABLET in 1 BOTTLE (63629-4838-1) |
NDC Code | 63629-4838-1 |
Proprietary Name | Hyoscyamine Sulfate |
Package Description | 20 TABLET in 1 BOTTLE (63629-4838-1) |
Product NDC | 63629-4838 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Hyoscyamine Sulfate |
Dosage Form Name | TABLET |
Route Name | ORAL; SUBLINGUAL |
Start Marketing Date | 20090921 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Bryant Ranch Prepack |
Substance Name | HYOSCYAMINE SULFATE |
Strength Number | .125 |
Strength Unit | mg/1 |
Pharmaceutical Classes |