FDA NDC Directory · JSON-LD · Markdown
NDC 43598-110 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE
| Generic name | Guaifenesin |
|---|---|
| Labeler / Manufacturer | Dr. Reddy's Laboratories Inc. |
| Marketing category | Abbreviated NDA (generic) · App ANDA215932 |
| Dosage form / route | TABLET, EXTENDED RELEASE · ORAL |
| Active ingredients | GUAIFENESIN (600 mg/1) |
| Marketing started | 20220901 |
| Package count | 1 |
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