Mucus
- Product NDC
- 62011-0347
- 11-digit product format
- 620110347
- Labeler code
- 62011
- Product ID
- 62011-0347_6a8cb47e-cbf8-4509-bf5d-a4fdbe002f26
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- MCKESSON (HEALTH MART)
- Application
- NDA021282
- Marketing category
- NDA
- Marketing start
- 2018-02-08
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 600 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 62011-0347-1 | Mucus | 20 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 20 | | 3 |
| 62011-0347-1 | Mucus | 1 in 1 CARTON | TABLET, EXTENDED RELEASE | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62011-0347 | MUCUS (GUAIFENESIN) TABLET, EXTENDED RELEASE [MCKESSON (HEALTH MART)] | 3 | Legacy NDC, 2 package rows | 20180208_ba3de8ce-4e83-4fa8-839e-fd9bfad83725.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 62011-0347-1 | 62011034701 | 20 in 1 BLISTER PACK | Historical |