Mucinex
- Product NDC
- 67296-0569
- 11-digit product format
- 672960569
- Labeler code
- 67296
- Product ID
- 67296-0569_bdae80ef-3eac-7455-e053-2a95a90a410c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- NDA021282
- Marketing category
- NDA
- Marketing start
- 2012-07-03
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 600 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-0569-1 | Mucinex | 20 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 20 | | 3 |
| 67296-0569-7 | Mucinex | 14 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 14 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0569 | MUCINEX (GUAIFENESIN) TABLET, EXTENDED RELEASE [REDPHARM DRUG, INC.] | 3 | Legacy NDC, 2 package rows | 20240823_bdae8726-ff98-4866-e053-2995a90ad67a.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 |
|---|
| 67296-0569-1 | 67296056901 | 20 in 1 BOTTLE | | | | | Historical |
| 67296-0569-7 | 67296056907 | 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-0569-7) | 2012-07-03 | 0000-00-00 | No | No | Current |