Mucinex
- Product NDC
- 55700-489
- 11-digit product format
- 557000489
- Labeler code
- 55700
- Product ID
- 55700-489_cd9ea5f2-fa10-4fcd-b005-8fad5c8effd6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- NDA021282
- Marketing category
- NDA
- Marketing start
- 2012-07-03
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 600 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record