mucus relief
- Product NDC
- 41250-684
- 11-digit product format
- 412500684
- Labeler code
- 41250
- Product ID
- 41250-684_097a3c6e-37e9-4380-ab8e-f458058014f4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, MULTILAYER, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Meijer Distribution Inc
- Application
- ANDA078912
- Marketing category
- ANDA
- Marketing start
- 2020-08-07
- 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
- 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 |
|---|
| 41250-684-02 | 41250068402 | 5 BLISTER PACK in 1 CARTON (41250-684-02) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK | 5 blister pack | 2021-09-15 | No | No | Historical |
| 41250-684-58 | 41250068458 | 1 BOTTLE in 1 CARTON (41250-684-58) / 40 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2020-08-19 | No | No | Historical |
| 41250-684-60 | 41250068460 | 1 BOTTLE in 1 CARTON (41250-684-60) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2020-08-07 | No | No | Historical |