mucus relief
- Product NDC
- 11822-2123
- 11-digit product format
- 118222123
- Labeler code
- 11822
- Product ID
- 11822-2123_f1887ccc-2d2a-4c36-8cca-1d2f22199495
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- guaifenesin
- Dosage form
- TABLET, MULTILAYER, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA078912
- Marketing category
- ANDA
- Marketing start
- 2022-12-05
- Marketing end
- 2026-09-30
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- mucus relief
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GUAIFENESIN | 600 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 495W7451VQ |
| Rxcui | 636522 |
DailyMed Product Concepts#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-2123-0 | 11822212300 | 1 BLISTER PACK in 1 CARTON (11822-2123-0) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK | 1 blister pack | 2023-04-12 | | No | No | Historical |
| 11822-2123-1 | 11822212301 | 2 BLISTER PACK in 1 CARTON (11822-2123-1) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK | 2 blister pack | 2022-12-05 | 0000-00-00 | No | No | Current |