Home
>
National Drug Code (NDC)
>
Chenodiol
Chenodiol - 0722-7121-01 - (Chenodiol)
Drug Information of Chenodiol
| Product NDC: | 0722-7121 |
| Proprietary Name: | Chenodiol |
| Non Proprietary Name: | Chenodiol |
| Active Ingredient(s): | 250 mg/1 & nbsp; Chenodiol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Chenodiol
| Product NDC: | 0722-7121 |
| Labeler Name: | Nexgen Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091019 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091001 |
Package Information of Chenodiol
| Package NDC: | 0722-7121-01 |
| Package Description: | 1 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0722-7121-01) |
NDC Information of Chenodiol
| NDC Code | 0722-7121-01 |
| Proprietary Name | Chenodiol |
| Package Description | 1 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0722-7121-01) |
| Product NDC | 0722-7121 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Chenodiol |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20091001 |
| Marketing Category Name | ANDA |
| Labeler Name | Nexgen Pharma, Inc. |
| Substance Name | CHENODIOL |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
