Azli Diluent
Azli Diluent
sodium chloride inhalation solution
AZLI DILUENT
sodium chloride inhalation solution inhalant |
| Product Information |
| Product Type | HUMAN PRESCRIPTION DRUG | Item Code (Source) | NDC: 60940-021 |
| Route of Administration | RESPIRATORY (INHALATION) |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) | SODIUM CHLORIDE | 1.7 mg in 1 mL |
|
| Inactive Ingredients |
| Ingredient Name | Strength |
| Water (UNII: 059QF0KO0R) | |
|
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 60940-021-01 | 45 in 1 PACKAGE | 12/01/2020 | |
| 1 | | 44 in 1 BOX | | |
| 1 | | 1 mL in 1 AMPULE; Type 0: Not a Combination Product | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved drug other | | 12/01/2020 | |
|
| Labeler - Holopack Verpackungstechnik GmbH
(313222457)
|
| Establishment |
| Name | Address | ID/FEI | Business Operations |
| Holopack Verpackungstechnik GmbH | | 343390324 | manufacture(60940-021) |