NDC 42549-609 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 42549-609 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA089160 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-04-22 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA089160 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-04-22 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA089160 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2010-04-22 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA089160 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-04-22 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA089160 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-04-22 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA089160 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-04-22 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA089160 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2010-04-22 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA089160 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-04-22 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA089160 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-04-22 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA089160 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-04-22 |
Inactivation Date | 2019-11-13 |