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URSO
URSO - 55154-1855-0 - (ursodiol)
Drug Information of URSO
| Product NDC: | 55154-1855 |
| Proprietary Name: | URSO |
| Non Proprietary Name: | ursodiol |
| Active Ingredient(s): | 250 mg/1 & nbsp; ursodiol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of URSO
| Product NDC: | 55154-1855 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020675 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19971210 |
Package Information of URSO
| Package NDC: | 55154-1855-0 |
| Package Description: | 10 POUCH in 1 BAG (55154-1855-0) > 1 TABLET, FILM COATED in 1 POUCH |
NDC Information of URSO
| NDC Code | 55154-1855-0 |
| Proprietary Name | URSO |
| Package Description | 10 POUCH in 1 BAG (55154-1855-0) > 1 TABLET, FILM COATED in 1 POUCH |
| Product NDC | 55154-1855 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ursodiol |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19971210 |
| Marketing Category Name | NDA |
| Labeler Name | Cardinal Health |
| Substance Name | URSODIOL |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Bile Acid [EPC],Bile Acids and Salts [Chemical/Ingredient] |
