Mucus Relief
- Product NDC
- 42507-253
- 11-digit product format
- 425070253
- Labeler code
- 42507
- Product ID
- 42507-253_484bfd9d-d3be-09f0-e063-6394a90a5eb1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- HYVEE INC
- Application
- ANDA213420
- Marketing category
- ANDA
- Marketing start
- 2026-01-13
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Mucus Relief
- Listing expiration
- 2027-12-31
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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42507-253-03 | Mucus Relief | 20 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 20 | | 2 |
| 42507-253-03 | Mucus Relief | 2 in 1 CARTON | TABLET, EXTENDED RELEASE | 2 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 42507-253-03 | 42507025303 | 2 BLISTER PACK in 1 CARTON (42507-253-03) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 2 blister pack | 2026-01-13 | No | No | Historical |