NDC 0603-3881 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0603-3881 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA089971 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1988-12-02 |
Marketing End Date | 2013-12-31 |
Marketing Category | ANDA |
Application Number | ANDA089971 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1988-12-02 |
Marketing End Date | 2013-12-31 |
Marketing Category | ANDA |
Application Number | ANDA089971 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1988-12-02 |
Marketing End Date | 2013-12-31 |
Marketing Category | ANDA |
Application Number | ANDA089971 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1988-12-02 |
Marketing End Date | 2013-12-31 |
Marketing Category | ANDA |
Application Number | ANDA089971 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2010-04-26 |
Marketing End Date | 2013-12-31 |
Marketing Category | ANDA |
Application Number | ANDA089971 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1988-12-02 |
Marketing End Date | 2013-12-31 |
Marketing Category | ANDA |
Application Number | ANDA089971 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1988-12-02 |
Marketing End Date | 2013-12-31 |
Marketing Category | ANDA |
Application Number | ANDA089971 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1988-12-02 |
Marketing End Date | 2013-12-31 |
Marketing Category | ANDA |
Application Number | ANDA089971 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1988-12-02 |
Marketing End Date | 2013-12-31 |
Marketing Category | ANDA |
Application Number | ANDA089971 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1988-12-02 |
Marketing End Date | 2013-12-31 |
Marketing Category | ANDA |
Application Number | ANDA089971 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1988-12-02 |
Marketing End Date | 2013-12-31 |