NDC 68387-520 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 68387-520 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA040336 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-08-29 |
Inactivation Date | 2019-10-21 |
Marketing Category | ANDA |
Application Number | ANDA040336 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-08-29 |
Inactivation Date | 2019-10-21 |
Marketing Category | ANDA |
Application Number | ANDA040336 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-08-29 |
Inactivation Date | 2019-10-21 |
Marketing Category | ANDA |
Application Number | ANDA040336 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-08-29 |
Inactivation Date | 2019-10-21 |