Mucus DM
- Product NDC
- 41250-735
- 11-digit product format
- 412500735
- Labeler code
- 41250
- Product ID
- 41250-735_d58caf3a-5d37-4983-99ee-fff4146087e6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dextromethorphan HBr, Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Meijer Distribution Inc
- Application
- ANDA091070
- Marketing category
- ANDA
- Marketing start
- 2016-07-29
- Marketing end
- 0000-00-00
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
- Active strength
- 60 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record