Mucus Relief Extended Release
NDC 11673-732, Guaifenesin, tablet, from TARGET Corporation.
- Product NDC
- 11673-732
- Status
- Listed
- Labeler
- TARGET Corporation
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA207342
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/11673-732 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- GUAIFENESIN1200 mg/1
Pharmacologic classes
Decreased Respiratory Secretion Viscosity [PE]; Expectorant [EPC]; Increased Respiratory Secretions [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 11673-732-14 | 11673073214 | 14 BLISTER PACK in 1 CARTON (11673-732-14) / 1 TABLET in 1 BLISTER PACK |
| 11673-732-28 | 11673073228 | 28 BLISTER PACK in 1 CARTON (11673-732-28) / 1 TABLET in 1 BLISTER PACK |
Linked data
RxNorm, label and prices
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 11673-732 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/11673-732 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 11673-732. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.