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Hyoscyamine Sulfate
Hyoscyamine Sulfate - 0574-0251-01 - (Hyoscyamine Sulfate)
Drug Information of Hyoscyamine Sulfate
| Product NDC: | 0574-0251 |
| 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, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hyoscyamine Sulfate
| Product NDC: | 0574-0251 |
| Labeler Name: | Paddock Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED OTHER |
| Start Marketing Date: | 20090919 |
Package Information of Hyoscyamine Sulfate
| Package NDC: | 0574-0251-01 |
| Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0574-0251-01) |
NDC Information of Hyoscyamine Sulfate
| NDC Code | 0574-0251-01 |
| Proprietary Name | Hyoscyamine Sulfate |
| Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0574-0251-01) |
| Product NDC | 0574-0251 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hyoscyamine Sulfate |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20090919 |
| Marketing Category Name | UNAPPROVED OTHER |
| Labeler Name | Paddock Laboratories, Inc. |
| Substance Name | HYOSCYAMINE SULFATE |
| Strength Number | .375 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
