NDC 71335-0553 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 71335-0553 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA090642 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2016-06-08 |
Marketing End Date | 2017-12-31 |
Marketing Category | ANDA |
Application Number | ANDA090642 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-06-08 |
Marketing End Date | 2017-12-31 |
Marketing Category | ANDA |
Application Number | ANDA090642 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2016-06-08 |
Marketing End Date | 2017-12-31 |
Marketing Category | ANDA |
Application Number | ANDA090642 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2016-06-08 |
Marketing End Date | 2017-12-31 |
Marketing Category | ANDA |
Application Number | ANDA090642 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2016-06-08 |
Marketing End Date | 2017-12-31 |
Marketing Category | ANDA |
Application Number | ANDA090642 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2016-06-08 |
Marketing End Date | 2017-12-31 |
Marketing Category | ANDA |
Application Number | ANDA090642 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-06-08 |
Marketing End Date | 2017-12-31 |