mucus relief
- Product NDC
- 41250-654
- 11-digit product format
- 412500654
- Labeler code
- 41250
- Product ID
- 41250-654_2905b83e-ae8f-43c4-9f59-291d8b717dea
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- guaifenesin
- Dosage form
- TABLET, MULTILAYER, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Meijer Distribution Inc
- Application
- ANDA213420
- Marketing category
- ANDA
- Marketing start
- 2021-02-23
- Marketing end
- 2026-10-01
- Substance
- GUAIFENESIN
- Active strength
- 1200 mg/1
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
- NDC exclude flag
- No
- 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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 41250-654-02 | 41250065402 | 3 BLISTER PACK in 1 CARTON (41250-654-02) / 14 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK | 3 blister pack | 2021-02-23 | 2026-10-01 | No | No | Historical |
| 41250-654-74 | 41250065474 | 1 BLISTER PACK in 1 CARTON (41250-654-74) / 14 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK | 1 blister pack | 2021-02-23 | 2026-10-01 | No | No | Historical |