NDC 55065-001 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 55065-001 |
Marketing Category | / |
Marketing Category | unapproved medical gas |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1986-01-02 |
Inactivation Date | 2019-10-21 |
Marketing Category | unapproved medical gas |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1986-01-02 |
Inactivation Date | 2019-10-21 |
Marketing Category | unapproved medical gas |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1986-01-02 |
Inactivation Date | 2019-10-21 |
Marketing Category | unapproved medical gas |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1986-01-02 |
Inactivation Date | 2019-10-21 |
Marketing Category | unapproved medical gas |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1986-01-02 |
Inactivation Date | 2019-10-21 |
Marketing Category | unapproved medical gas |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1986-01-02 |
Inactivation Date | 2019-10-21 |