Mucus Relief
- Product NDC
- 83324-096
- 11-digit product format
- 833240096
- Labeler code
- 83324
- Product ID
- 83324-096_1f19e82a-7d42-53c4-e063-6294a90ae19a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- CHAIN DRUG MARKETING ASSOCIATION, INC.
- Application
- ANDA213420
- Marketing category
- ANDA
- Marketing start
- 2024-08-07
- 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 |
|---|
| 83324-096-14 | 83324009614 | 1 BLISTER PACK in 1 CARTON (83324-096-14) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 1 blister pack | 2024-08-07 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| 1204A-QCH-2024-0807 | CHAIN DRUG MARKETING ASSOCIATION, INC. | 2024-08-07 | HUMAN OTC DRUG LABEL | 2 |