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URSODIOL
URSODIOL - 64980-139-01 - (URSODIOL)
Drug Information of URSODIOL
| Product NDC: | 64980-139 |
| Proprietary Name: | URSODIOL |
| Non Proprietary Name: | URSODIOL |
| Active Ingredient(s): | 300 mg/1 & nbsp; URSODIOL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of URSODIOL
| Product NDC: | 64980-139 |
| Labeler Name: | Rising Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077895 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20061005 |
Package Information of URSODIOL
| Package NDC: | 64980-139-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE, PLASTIC (64980-139-01) |
NDC Information of URSODIOL
| NDC Code | 64980-139-01 |
| Proprietary Name | URSODIOL |
| Package Description | 100 CAPSULE in 1 BOTTLE, PLASTIC (64980-139-01) |
| Product NDC | 64980-139 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | URSODIOL |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20061005 |
| Marketing Category Name | ANDA |
| Labeler Name | Rising Pharmaceuticals, Inc. |
| Substance Name | URSODIOL |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Bile Acid [EPC],Bile Acids and Salts [Chemical/Ingredient] |
