mucus D
- Product NDC
- 79481-0119
- 11-digit product format
- 794810119
- Labeler code
- 79481
- Product ID
- 79481-0119_1310817a-11f3-41f5-a041-299d92a56555
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- guaifenesin and pseudoephedrine hydrochloride
- Dosage form
- TABLET, MULTILAYER, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Meijer, Inc.
- Application
- ANDA214407
- Marketing category
- ANDA
- Marketing start
- 2023-08-22
- Substance
- GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE
- Active strength
- 1200; 120 mg/1; mg/1
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-Adrenergic Agonist [EPC]
- 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 |
| 6V9V2RYJ8N | PSEUDOEPHEDRINE HYDROCHLORIDE | 345-78-8 | PSEUDOEPHEDRINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 79481-0119-0 | 79481011900 | 4 BLISTER PACK in 1 CARTON (79481-0119-0) / 6 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK | 4 blister pack | 2023-08-22 | No | No | Historical |