Up and Up mucus relief
- Product NDC
- 11673-325
- 11-digit product format
- 116730325
- Labeler code
- 11673
- Product ID
- 11673-325_8efb699e-e4a9-4e6a-9d14-35b39035fa4e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA091009
- Marketing category
- ANDA
- Marketing start
- 2016-07-11
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 1200 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 |
|---|
| 11673-325-30 | Up and Up mucus relief | 28 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 28 | | 2 |
| 11673-325-30 | Up and Up mucus relief | 1 in 1 CARTON | TABLET, EXTENDED RELEASE | 1 | | 2 |
| 11673-325-66 | Up and Up mucus relief | 1 in 1 CARTON | TABLET, EXTENDED RELEASE | 1 | | 2 |
| 11673-325-66 | Up and Up mucus relief | 14 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 14 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-325 | UP AND UP MUCUS RELIEF (GUAIFENESIN) TABLET, EXTENDED RELEASE [TARGET CORPORATION] | 2 | Legacy NDC, 4 package rows | 20191109_9c29d93e-6df0-4b2f-a179-deae1f64eaa4.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 11673-325-30 | 11673032530 | 28 in 1 BOTTLE | Historical |
| 11673-325-66 | 11673032566 | 1 in 1 CARTON | Historical |