CROMOLYN SODIUM- cromolyn sodium powder
AX Pharmaceutical Corp
----------
Cromolyn sodium
Cromolyn sodium

CROMOLYN SODIUM
cromolyn sodium powder |
| Product Information |
| Product Type | | Item Code (Source) | NDC: 73377-122 |
| Route of Administration | NOT APPLICABLE |
|
| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| CROMOLYN SODIUM (UNII: Q2WXR1I0PK) (CROMOLYN SODIUM - UNII:Q2WXR1I0PK) | CROMOLYN SODIUM | 1 g in 1 g |
|
| Product Characteristics |
| Color | white | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
|
| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 73377-122-01 | 100 g in 1 JAR | | |
|
|
| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| bulk ingredient for animal drug compounding | | 04/05/2021 | 07/03/2025 |
|
| Labeler - AX Pharmaceutical Corp
(204011316)
|
| Establishment |
| Name | Address | ID/FEI | Business Operations |
| AX Pharmaceutical Corp | | 204011316 | repack, relabel |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.