Mucus Relief DM
- Product NDC
- 68016-550
- 11-digit product format
- 680160550
- Labeler code
- 68016
- Product ID
- 68016-550_a42ddeef-7b22-45d8-9af5-fac2b97b5e43
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dextromethorphan HBr and Guaifenesin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Chain Drug Consortium
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2023-01-12
- Marketing end
- 0000-00-00
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
- Active strength
- 20 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
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68016-550 | MUCUS RELIEF DM (DEXTROMETHORPHAN HBR AND GUAIFENESIN) TABLET, FILM COATED [CHAIN DRUG CONSORTIUM] | 4 | Legacy NDC | 20250108_9e32e9a9-b378-4f1d-82c4-c1769954fc10.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68016-550-50 | 68016055050 | 1 BOTTLE, PLASTIC in 1 CARTON (68016-550-50) > 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 2023-01-12 | 0000-00-00 | No | No | Current |