FDA NDC Directory · JSON-LD · Markdown
NDC 70954-522 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION
| Generic name | hydrochlorothiazide |
|---|---|
| Labeler / Manufacturer | ANI Pharmaceuticals, Inc. |
| Marketing category | New Drug Application (innovator) · App NDA219141 |
| Dosage form / route | POWDER, FOR SUSPENSION · ORAL |
| Active ingredients | HYDROCHLOROTHIAZIDE (10 mg/mL) |
| Marketing started | 20250130 |
| Package count | 1 |
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