Mucus Relief
- Product NDC
- 59726-237
- 11-digit product format
- 597260237
- Labeler code
- 59726
- Product ID
- 59726-237_885e0a80-bf98-4f71-a04f-1e94a30a8362
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- ANDA207342
- Marketing category
- ANDA
- Marketing start
- 2025-02-15
- Substance
- GUAIFENESIN
- Active strength
- 1200 mg/1
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 495W7451VQ | GUAIFENESIN | 93-14-1 | GUAIFENESIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 59726-237-07 | 59726023707 | 7 BLISTER PACK in 1 CARTON (59726-237-07) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 7 blister pack | 2025-02-15 | No | No | Historical |
| 59726-237-14 | 59726023714 | 14 BLISTER PACK in 1 CARTON (59726-237-14) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 14 blister pack | 2025-02-15 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Drug Facts | P & L Development, LLC | 2025-02-12 | HUMAN OTC DRUG LABEL | 2 |