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 |