Mucus
- Product NDC
- 49035-070
- 11-digit product format
- 490350070
- Labeler code
- 49035
- Product ID
- 49035-070_b9963b79-2226-415a-a165-c5f39a43e511
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- WALMART STORES, INC.
- 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
- 2020-12-31
- 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 |
|---|
| 49035-070-21 | Mucus | 1 in 1 CARTON | TABLET, EXTENDED RELEASE | 1 | | 5 |
| 49035-070-21 | Mucus | 20 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 20 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49035-070 | MUCUS (GUAIFENESIN) TABLET, EXTENDED RELEASE [WALMART STORES, INC.] | 5 | Legacy NDC, 2 package rows | 20190620_1b7cf796-8571-4ba1-be27-c00280c5f845.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 |
|---|
| 49035-070-21 | 49035007021 | 1 BLISTER PACK in 1 CARTON (49035-070-21) > 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 1 blister pack | 2018-02-08 | 0000-00-00 | No | No | Current |