Mucinex DM
- Product NDC
- 50090-2298
- 11-digit product format
- 500902298
- Labeler code
- 50090
- Product ID
- 50090-2298_3e3ff864-5916-412c-a5bd-a7c28eb1e775
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin and Dextromethorphan Hydrobromide
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA021620
- Marketing category
- NDA
- Marketing start
- 2012-06-26
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE
- Active strength
- 1200 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 50090-2298-0 | 50090229800 | 1 BLISTER PACK in 1 CARTON (50090-2298-0) > 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 1 blister pack | 2016-02-11 | 0000-00-00 | No | No | Current |