Mucus
- Product NDC
- 30142-701
- 11-digit product format
- 301420701
- Labeler code
- 30142
- Product ID
- 30142-701_09d93ec2-f597-4038-8d97-7530bc85faba
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- KROGER COMPANY
- Application
- NDA021282
- Marketing category
- NDA
- Marketing start
- 2017-09-07
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 600 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 30142-701-20 | Mucus | 1 in 1 CARTON | TABLET, EXTENDED RELEASE | 1 | | 5 |
| 30142-701-20 | 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 |
|---|
| 30142-701 | MUCUS (GUAIFENESIN) TABLET, EXTENDED RELEASE [KROGER COMPANY] | 5 | Legacy NDC, 2 package rows | 20200213_20aa5ec5-d14e-4418-b9b9-d7c5c16de80b.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 |
|---|
| 30142-701-20 | 30142070120 | 1 BLISTER PACK in 1 CARTON (30142-701-20) > 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 1 blister pack | 2017-09-07 | 0000-00-00 | No | No | Current |