FdaApplication
NDA 016211
Identifiers
- fda_app_no: NDA016211
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | NDA |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MIOCHOL | ACETYLCHOLINE CHLORIDE | 20MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | FOR SOLUTION;OPHTHALMIC |
1 product