Product NDC: | 43199-014 |
Proprietary Name: | Hyoscyamine Sulfate Extended-Release |
Non Proprietary Name: | Hyoscyamine Sulfate Extended-Release |
Active Ingredient(s): | .375 mg/1 & nbsp; Hyoscyamine Sulfate Extended-Release |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43199-014 |
Labeler Name: | County Line Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20100103 |
Package NDC: | 43199-014-01 |
Package Description: | 100 TABLET in 1 BOTTLE (43199-014-01) |
NDC Code | 43199-014-01 |
Proprietary Name | Hyoscyamine Sulfate Extended-Release |
Package Description | 100 TABLET in 1 BOTTLE (43199-014-01) |
Product NDC | 43199-014 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Hyoscyamine Sulfate Extended-Release |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100103 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | County Line Pharmaceuticals, LLC |
Substance Name | HYOSCYAMINE SULFATE |
Strength Number | .375 |
Strength Unit | mg/1 |
Pharmaceutical Classes |