Mucus DM Extended-Release
- Product NDC
- 59726-834
- 11-digit product format
- 597260834
- Labeler code
- 59726
- Product ID
- 59726-834_b4df16e9-d913-4d5b-820b-213bf32445e7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dextromethorphan Hydrobromide and Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- ANDA209692
- Marketing category
- ANDA
- Marketing start
- 2019-01-01
- Marketing end
- 0000-00-00
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
- Active strength
- 60 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 59726-834-14 | 59726083414 | 14 BLISTER PACK in 1 CARTON (59726-834-14) > 1 TABLET in 1 BLISTER PACK | 14 blister pack | 2019-01-01 | 0000-00-00 | No | No | Current |