FDA NDC Directory · JSON-LD · Markdown
NDC 51672-2115 · HUMAN OTC DRUG · SUPPOSITORY
| Generic name | Acetaminophen |
|---|---|
| Labeler / Manufacturer | Sun Pharmaceutical Industries, Inc. |
| Marketing category | New Drug Application (innovator) · App NDA018337 |
| Dosage form / route | SUPPOSITORY · RECTAL |
| Active ingredients | ACETAMINOPHEN (120 mg/1) |
| Marketing started | 20131212 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).