NDC 54868-5650 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 54868-5650 | 
| Marketing Category | / | 
| Marketing Category | ANDA | 
| Application Number | ANDA077927 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2006-08-07 | 
| Inactivation Date | 2019-09-24 | 
| Marketing Category | ANDA | 
| Application Number | ANDA077927 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2006-08-07 | 
| Inactivation Date | 2019-09-24 | 
| Marketing Category | ANDA | 
| Application Number | ANDA077927 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2006-08-07 | 
| Inactivation Date | 2019-09-24 | 
| Marketing Category | ANDA | 
| Application Number | ANDA077927 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2011-02-22 | 
| Inactivation Date | 2019-09-24 | 
| Marketing Category | ANDA | 
| Application Number | ANDA077927 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2006-08-07 | 
| Inactivation Date | 2019-09-24 | 
| Marketing Category | ANDA | 
| Application Number | ANDA077927 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2006-08-07 | 
| Inactivation Date | 2019-09-24 | 
| Marketing Category | ANDA | 
| Application Number | ANDA077927 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2010-10-01 | 
| Inactivation Date | 2019-09-24 |