Mucinex DM
- Product NDC
- 60687-651
- 11-digit product format
- 606870651
- Labeler code
- 60687
- Product ID
- 60687-651_dd44a472-a2a1-347b-e053-2995a90af3d5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin and Dextromethorphan Hydrobromide
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- NDA021620
- Marketing category
- NDA
- Marketing start
- 2022-04-14
- Marketing end
- 0000-00-00
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
- Active strength
- 30 mg/1; mg/1
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-651-21 | 60687065121 | 30 BLISTER PACK in 1 CARTON (60687-651-21) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-651-11) | 30 blister pack | 2022-04-14 | 0000-00-00 | No | No | Current |