NDC 68387-100 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68387-100 | 
| Marketing Category | / | 
| Marketing Category | ANDA | 
| Application Number | ANDA074843 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2009-03-01 | 
| Inactivation Date | 2019-10-21 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074843 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2009-03-01 | 
| Inactivation Date | 2019-10-21 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074843 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2009-03-01 | 
| Inactivation Date | 2019-10-21 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074843 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2009-03-01 | 
| Inactivation Date | 2019-10-21 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074843 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2009-03-01 | 
| Inactivation Date | 2019-10-21 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074843 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2009-03-01 | 
| Inactivation Date | 2019-10-21 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074843 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2009-03-01 | 
| Inactivation Date | 2019-10-21 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074843 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2009-03-01 | 
| Inactivation Date | 2019-10-21 |