mucus er
- Product NDC
- 42507-202
- 11-digit product format
- 425070202
- Labeler code
- 42507
- Product ID
- 42507-202_ee44f332-091f-4430-b04e-bd2fcb42fb9f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- guaifenesin
- Dosage form
- TABLET, MULTILAYER, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- HyVee Inc
- Application
- ANDA078912
- Marketing category
- ANDA
- Marketing start
- 2026-01-28
- 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 er
- 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 |
|---|
| 42507-202-12 | mucus er | 20 in 1 BOTTLE | TABLET, MULTILAYER, EXTENDED REL | 20 | | 2 |
| 42507-202-60 | mucus er | 1 in 1 CARTON | TABLET, MULTILAYER, EXTENDED REL | 1 | | 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 |
|---|
| 42507-202-12 | 42507020212 | 20 in 1 BOTTLE | | | | | Historical |
| 42507-202-60 | 42507020260 | 1 BOTTLE in 1 CARTON (42507-202-60) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE (42507-202-12) | 1 bottle | 2026-01-28 | No | No | Historical |