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Hyoscyamine Sulfate
Hyoscyamine Sulfate - 43063-321-60 - (Hyoscyamine Sulfate)
Drug Information of Hyoscyamine Sulfate
| Product NDC: | 43063-321 |
| Proprietary Name: | Hyoscyamine Sulfate |
| Non Proprietary Name: | Hyoscyamine Sulfate |
| Active Ingredient(s): | .125 mg/1 & nbsp; Hyoscyamine Sulfate |
| Administration Route(s): | ORAL; SUBLINGUAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hyoscyamine Sulfate
| Product NDC: | 43063-321 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20090921 |
Package Information of Hyoscyamine Sulfate
| Package NDC: | 43063-321-60 |
| Package Description: | 60 TABLET in 1 BOTTLE, PLASTIC (43063-321-60) |
NDC Information of Hyoscyamine Sulfate
| NDC Code | 43063-321-60 |
| Proprietary Name | Hyoscyamine Sulfate |
| Package Description | 60 TABLET in 1 BOTTLE, PLASTIC (43063-321-60) |
| Product NDC | 43063-321 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hyoscyamine Sulfate |
| Dosage Form Name | TABLET |
| Route Name | ORAL; SUBLINGUAL |
| Start Marketing Date | 20090921 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | HYOSCYAMINE SULFATE |
| Strength Number | .125 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
