Product NDC: | 50532-112 |
Proprietary Name: | Hyoscyamine Sulfate |
Non Proprietary Name: | HYOSCYAMINE SULFATE |
Active Ingredient(s): | .125 mg/1 & nbsp; HYOSCYAMINE SULFATE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50532-112 |
Labeler Name: | Franklin Pharmaceutical LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20100501 |
Package NDC: | 50532-112-10 |
Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (50532-112-10) |
NDC Code | 50532-112-10 |
Proprietary Name | Hyoscyamine Sulfate |
Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (50532-112-10) |
Product NDC | 50532-112 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | HYOSCYAMINE SULFATE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100501 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Franklin Pharmaceutical LLC |
Substance Name | HYOSCYAMINE SULFATE |
Strength Number | .125 |
Strength Unit | mg/1 |
Pharmaceutical Classes |