FdaApplication
NDA 050719
Identifiers
- fda_app_no: NDA050719
Properties
| Property | Value |
|---|---|
| applicant_name | CASPER PHARMA LLC |
| application_type | NDA |
| approval_date | 1996-08-15 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HELIDAC | BISMUTH SUBSALICYLATE; METRONIDAZOLE; TETRACYCLINE HYDROCHLORIDE | 262.4MG,N/A,N/A;N/A,250MG,N/A;N/A,N/A,500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, CHEWABLE, TABLET, CAPSULE;ORAL |
1 product