Product NDC: | 13925-108 |
Proprietary Name: | Hyoscyamine |
Non Proprietary Name: | Hyoscyamine |
Active Ingredient(s): | .375 mg/1 & nbsp; Hyoscyamine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 13925-108 |
Labeler Name: | Seton Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20120301 |
Package NDC: | 13925-108-01 |
Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (13925-108-01) |
NDC Code | 13925-108-01 |
Proprietary Name | Hyoscyamine |
Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (13925-108-01) |
Product NDC | 13925-108 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Hyoscyamine |
Dosage Form Name | TABLET, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20120301 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Seton Pharmaceuticals |
Substance Name | HYOSCYAMINE SULFATE |
Strength Number | .375 |
Strength Unit | mg/1 |
Pharmaceutical Classes |