Mucus Relief DM
- Product NDC
- 62011-0423
- 11-digit product format
- 620110423
- Labeler code
- 62011
- Product ID
- 62011-0423_ac01899c-3789-4e38-bb69-85b752b98384
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin, Dextromethorphan HBr
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA209692
- Marketing category
- ANDA
- Marketing start
- 2019-11-29
- Marketing end
- 0000-00-00
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
- Active strength
- 60 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 |
|---|
| 62011-0423-1 | 62011042301 | 14 BLISTER PACK in 1 CARTON (62011-0423-1) > 1 TABLET in 1 BLISTER PACK | 14 blister pack | 2019-11-29 | 0000-00-00 | No | No | Current |