Mucinex
- Product NDC
- 70518-0228
- 11-digit product format
- 705180228
- Labeler code
- 70518
- Product ID
- 70518-0228_e715d126-cda5-ecc0-e053-2995a90a03a8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA021282
- Marketing category
- NDA
- Marketing start
- 2017-02-16
- 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 |
|---|
| 70518-0228-1 | 70518022801 | 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-0228-1) | 2017-02-27 | 0000-00-00 | No | No | Current |