Mucinex
- Product NDC
- 63187-954
- 11-digit product format
- 631870954
- Labeler code
- 63187
- Product ID
- 63187-954_d8381687-e02a-45ea-8a85-8c84874cf919
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- NDA021282
- Marketing category
- NDA
- Marketing start
- 2012-07-03
- Substance
- GUAIFENESIN
- Active strength
- 600 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Mucinex
- 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, 891301 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63187-954-20 | Mucinex | 20 in 1 CARTON | TABLET, EXTENDED RELEASE | 20 | | 4 |
| 63187-954-40 | Mucinex | 40 in 1 CARTON | TABLET, EXTENDED RELEASE | 40 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63187-954 | MUCINEX (GUAIFENESIN) TABLET, EXTENDED RELEASE [PROFICIENT RX LP] | 4 | Current NDC, Legacy NDC, 2 package rows | 20210112_f3ade814-2759-4ad0-a196-210e84d8cde9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-954-20 | 63187095420 | 20 TABLET, EXTENDED RELEASE in 1 CARTON (63187-954-20) | 2019-08-01 | 0000-00-00 | No | No | Current |
| 63187-954-40 | 63187095440 | 40 TABLET, EXTENDED RELEASE in 1 CARTON (63187-954-40) | 2018-01-01 | 0000-00-00 | No | No | Current |