NDC 42549-503 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 42549-503 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA040124 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1996-01-24 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA040124 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1996-01-24 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA040124 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1996-01-24 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA040124 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1996-01-24 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA040124 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1996-01-24 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA040124 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1996-01-24 |
Inactivation Date | 2019-11-13 |