NDC 0172-5663 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0172-5663 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA075385 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2002-03-02 |
Marketing End Date | 2012-04-30 |
Marketing Category | ANDA |
Application Number | ANDA075385 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2010-08-26 |
Marketing End Date | 2012-04-30 |
Marketing Category | ANDA |
Application Number | ANDA075385 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2002-03-02 |
Marketing End Date | 2012-03-16 |
Marketing Category | ANDA |
Application Number | ANDA075385 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2002-03-02 |
Marketing End Date | 2012-04-30 |
Marketing Category | ANDA |
Application Number | ANDA075385 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2002-03-02 |
Marketing End Date | 2012-03-16 |
Marketing Category | ANDA |
Application Number | ANDA075385 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2002-03-02 |
Marketing End Date | 2012-04-30 |