Mucinex
- Product NDC
- 55289-087
- 11-digit product format
- 552890087
- Labeler code
- 55289
- Product ID
- 55289-087_e5fd2b46-6841-4cf5-e053-2995a90a5512
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- NDA021282
- Marketing category
- NDA
- Marketing start
- 2012-07-03
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 600 mg/1
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55289-087-20 | 55289008720 | 20 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55289-087-20) | 2021-03-27 | 0000-00-00 | No | No | Current |