NDC 54868-4802 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 54868-4802 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA075509 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2003-05-28 |
Inactivation Date | 2019-09-24 |
Marketing Category | ANDA |
Application Number | ANDA075509 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2003-05-28 |
Inactivation Date | 2019-09-24 |
Marketing Category | ANDA |
Application Number | ANDA075509 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2003-05-28 |
Inactivation Date | 2019-09-24 |
Marketing Category | ANDA |
Application Number | ANDA075509 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2003-05-28 |
Inactivation Date | 2019-09-24 |
Marketing Category | ANDA |
Application Number | ANDA075509 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2003-05-28 |
Inactivation Date | 2019-09-24 |