Mucinex DM
- Product NDC
- 68788-6340
- 11-digit product format
- 687886340
- Labeler code
- 68788
- Product ID
- 68788-6340_e5a8b056-a250-482b-b820-f40f70ab467f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin and Dextromethorphan Hydrobromide
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- NDA021620
- Marketing category
- NDA
- Marketing start
- 2016-10-17
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE
- Active strength
- 600 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 68788-6340-2 | 68788634002 | 1 BLISTER PACK in 1 CARTON (68788-6340-2) > 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 1 blister pack | 2016-10-17 | 0000-00-00 | No | No | Current |