| Product NDC: | 50532-115 |
| Proprietary Name: | Hyoscyamine Sulfate |
| Non Proprietary Name: | HYOSCYAMINE SULFATE |
| Active Ingredient(s): | .375 mg/1 & nbsp; HYOSCYAMINE SULFATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50532-115 |
| Labeler Name: | Franklin Pharmaceutical LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100501 |
| Package NDC: | 50532-115-10 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (50532-115-10) |
| NDC Code | 50532-115-10 |
| Proprietary Name | Hyoscyamine Sulfate |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (50532-115-10) |
| Product NDC | 50532-115 |
| 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 | .375 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |