| Product NDC: | 0574-0250 |
| Proprietary Name: | HYOSCYAMINE SULFATE |
| Non Proprietary Name: | HYOSCYAMINE SULFATE |
| Active Ingredient(s): | .125 mg/1 & nbsp; HYOSCYAMINE SULFATE |
| Administration Route(s): | SUBLINGUAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0574-0250 |
| Labeler Name: | Paddock Laboratories, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120806 |
| Package NDC: | 0574-0250-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0574-0250-01) |
| NDC Code | 0574-0250-01 |
| Proprietary Name | HYOSCYAMINE SULFATE |
| Package Description | 100 TABLET in 1 BOTTLE (0574-0250-01) |
| Product NDC | 0574-0250 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HYOSCYAMINE SULFATE |
| Dosage Form Name | TABLET |
| Route Name | SUBLINGUAL |
| Start Marketing Date | 20120806 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Paddock Laboratories, LLC |
| Substance Name | HYOSCYAMINE SULFATE |
| Strength Number | .125 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |