Mucus Relief
- Product NDC
- 71335-2642
- 11-digit product format
- 713352642
- Labeler code
- 71335
- Product ID
- 71335-2642_bfd50410-1289-4b5d-86df-3b939d50bc27
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA209215
- Marketing category
- ANDA
- Marketing start
- 2019-09-23
- 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
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GUAIFENESIN | 600 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 495W7451VQ |
| Rxcui | 636522 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2642-1 | 71335264201 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-1) | 2025-06-02 | No | No | Historical |
| 71335-2642-2 | 71335264202 | 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-2) | 2025-06-02 | No | No | Historical |
| 71335-2642-3 | 71335264203 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-3) | 2025-06-02 | No | No | Historical |
| 71335-2642-4 | 71335264204 | 40 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-4) | 2025-06-02 | No | No | Historical |
| 71335-2642-5 | 71335264205 | 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-5) | 2025-06-02 | No | No | Historical |
| 71335-2642-6 | 71335264206 | 6 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-6) | 2025-06-02 | No | No | Historical |