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Hyoscyamine Sulfate
Hyoscyamine Sulfate - 21695-442-20 - (Hyoscyamine Sulfate)
Drug Information of Hyoscyamine Sulfate
| Product NDC: | 21695-442 |
| 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) |
Labeler Information of Hyoscyamine Sulfate
| Product NDC: | 21695-442 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20091105 |
Package Information of Hyoscyamine Sulfate
| Package NDC: | 21695-442-20 |
| Package Description: | 20 TABLET in 1 BOTTLE (21695-442-20) |
NDC Information of Hyoscyamine Sulfate
| NDC Code | 21695-442-20 |
| Proprietary Name | Hyoscyamine Sulfate |
| Package Description | 20 TABLET in 1 BOTTLE (21695-442-20) |
| Product NDC | 21695-442 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hyoscyamine Sulfate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091105 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | HYOSCYAMINE SULFATE |
| Strength Number | .125 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
