FDA NDC Directory · JSON-LD · Markdown
NDC 70954-909 · HUMAN PRESCRIPTION DRUG · TABLET
| Labeler / Manufacturer | ANI Pharmaceuticals, Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA219917 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | LOFEXIDINE HYDROCHLORIDE (.18 mg/1) |
| Marketing started | 20251022 |
| Package count | 2 |
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