Mucus Relief DM
- Product NDC
- 37012-729
- 11-digit product format
- 370120729
- Labeler code
- 37012
- Product ID
- 37012-729_b5fa7a35-5993-4285-951a-0b538638363c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin, Dextromethorphan HBr
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Shopko Stores Operating Co., LLC.
- Application
- ANDA209692
- Marketing category
- ANDA
- Marketing start
- 2018-12-31
- Marketing end
- 2022-12-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37012-729-28 | 37012072928 | 28 BLISTER PACK in 1 CARTON (37012-729-28) > 1 TABLET in 1 BLISTER PACK | 28 blister pack | 2018-12-31 | 0000-00-00 | No | No | Current |