FdaApplication
NDA 020021
Identifiers
- fda_app_no: NDA020021
Properties
| Property | Value |
|---|---|
| applicant_name | KENVUE BRANDS LLC |
| application_type | NDA |
| approval_date | 1992-12-15 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SUDAFED 24 HOUR | PSEUDOEPHEDRINE HYDROCHLORIDE | 240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, EXTENDED RELEASE;ORAL |
1 product