Mucinex
- Product NDC
- 29485-6647
- 11-digit product format
- 294856647
- Labeler code
- 29485
- Product ID
- 29485-6647_d208cdfd-3144-c730-e053-2a95a90a8c58
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Mechanical Servants LLC
- Application
- NDA021620
- Marketing category
- NDA
- Marketing start
- 2012-06-26
- Marketing end
- 0000-00-00
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
- Active strength
- 30 mg/1; 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 |
|---|
| 29485-6647-1 | MucinexDM | 1 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 1 | | 6 |
| 29485-6647-1 | MucinexDM | 2 in 1 POUCH | TABLET, EXTENDED RELEASE | 2 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 29485-6647 | MUCINEX DM (DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN) TABLET, EXTENDED RELEASE [MECHANICAL SERVANTS LLC] | 6 | Legacy NDC, 2 package rows | 20211216_0fc54199-9a61-4a63-b5cd-b132e44f23c9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 29485-6647-1 | 29485664701 | 1 POUCH in 1 BLISTER PACK (29485-6647-1) > 2 TABLET, EXTENDED RELEASE in 1 POUCH | 1 pouch | 2012-06-26 | 0000-00-00 | No | No | Current |
| 29485-6647-2 | 29485664702 | 2 TABLET, EXTENDED RELEASE in 1 POUCH (29485-6647-2) | | 2012-06-26 | 0000-00-00 | No | No | Current |