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Levsin
Levsin - 68220-113-50 - (hyoscyamine sulfate)
Drug Information of Levsin
| Product NDC: | 68220-113 |
| Proprietary Name: | Levsin |
| Non Proprietary Name: | hyoscyamine sulfate |
| Active Ingredient(s): | .125 mg/1 & nbsp; hyoscyamine sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Levsin
| Product NDC: | 68220-113 |
| Labeler Name: | Alaven Pharmaceutical LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20081201 |
Package Information of Levsin
| Package NDC: | 68220-113-50 |
| Package Description: | 500 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68220-113-50) |
NDC Information of Levsin
| NDC Code | 68220-113-50 |
| Proprietary Name | Levsin |
| Package Description | 500 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68220-113-50) |
| Product NDC | 68220-113 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hyoscyamine sulfate |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20081201 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Alaven Pharmaceutical LLC |
| Substance Name | HYOSCYAMINE SULFATE |
| Strength Number | .125 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
