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HYOSCYAMINE SULFATE
HYOSCYAMINE SULFATE - 60258-802-15 - (Hyoscyamine Sulfate)
Drug Information of HYOSCYAMINE SULFATE
| Product NDC: | 60258-802 |
| Proprietary Name: | HYOSCYAMINE SULFATE |
| Non Proprietary Name: | Hyoscyamine Sulfate |
| Active Ingredient(s): | .125 mg/mL & nbsp; Hyoscyamine Sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HYOSCYAMINE SULFATE
| Product NDC: | 60258-802 |
| Labeler Name: | Cypress Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20081230 |
Package Information of HYOSCYAMINE SULFATE
| Package NDC: | 60258-802-15 |
| Package Description: | 1 BOTTLE in 1 CARTON (60258-802-15) > 15 mL in 1 BOTTLE |
NDC Information of HYOSCYAMINE SULFATE
| NDC Code | 60258-802-15 |
| Proprietary Name | HYOSCYAMINE SULFATE |
| Package Description | 1 BOTTLE in 1 CARTON (60258-802-15) > 15 mL in 1 BOTTLE |
| Product NDC | 60258-802 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hyoscyamine Sulfate |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | ORAL |
| Start Marketing Date | 20081230 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Cypress Pharmaceutical, Inc. |
| Substance Name | HYOSCYAMINE SULFATE |
| Strength Number | .125 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
