LACTULOSE (LACTULOSE) — FDA Approval ANDA090502 (FRESENIUS KABI)
LACTULOSE (LACTULOSE) — FDA Approval ANDA090502 (FRESENIUS KABI) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: LACTULOSE; Active ingredients: LACTULOSE; Application number: ANDA090502.
| Brand name | LACTULOSE |
|---|---|
| Active ingredients | LACTULOSE |
| Application number | ANDA090502 |
| Sponsor | FRESENIUS KABI |
| Dosage form | SOLUTION |
| Route | ORAL, RECTAL |
| Marketing status | Prescription |
| Products in application | 1 |
| First approval date | 20120125 |
| Source | openFDA Drugs@FDA |
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