NDC 0603-2949 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0603-2949 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077856 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-06-28 |
Marketing End Date | 2018-02-28 |
Marketing Category | ANDA |
Application Number | ANDA077856 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-06-28 |
Marketing End Date | 2018-02-28 |
Marketing Category | ANDA |
Application Number | ANDA077856 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-06-28 |
Marketing End Date | 2018-02-28 |
Marketing Category | ANDA |
Application Number | ANDA077856 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-06-28 |
Marketing End Date | 2018-02-28 |
Marketing Category | ANDA |
Application Number | ANDA077856 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-06-28 |
Marketing End Date | 2018-02-28 |
Marketing Category | ANDA |
Application Number | ANDA077856 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-06-28 |
Marketing End Date | 2018-02-28 |
Marketing Category | ANDA |
Application Number | ANDA077856 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2006-06-28 |
Marketing End Date | 2016-05-20 |
Marketing Category | ANDA |
Application Number | ANDA077856 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-06-28 |
Marketing End Date | 2018-02-28 |
Marketing Category | ANDA |
Application Number | ANDA077856 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-06-28 |
Marketing End Date | 2018-02-28 |
Marketing Category | ANDA |
Application Number | ANDA077856 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-06-28 |
Marketing End Date | 2018-02-28 |