NDC 42549-549 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 42549-549 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA076280 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2002-11-26 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA076280 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2002-11-26 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA076280 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2002-11-26 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA076280 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2002-11-26 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA076280 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2002-11-26 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA076280 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2002-11-26 |
Inactivation Date | 2019-11-13 |