up and up maximum strength mucus relief dm
- Product NDC
- 11673-235
- 11-digit product format
- 116730235
- Labeler code
- 11673
- Product ID
- 11673-235_617ebd8b-85db-4a79-a9b3-877f77ffa75b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- dextromethorphan hydrobromide, guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA207602
- Marketing category
- ANDA
- Marketing start
- 2018-09-27
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE
- Active strength
- 1200 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-235 | UP AND UP MAXIMUM STRENGTH MUCUS RELIEF DM (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN) TABLET, EXTENDED RELEASE [TARGET CORPORATION] | 3 | Legacy NDC | 20200915_5bcb49ee-94c2-4624-824a-84213ab152b1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-235-30 | 11673023530 | 1 BOTTLE in 1 CARTON (11673-235-30) > 28 TABLET, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2018-09-27 | 0000-00-00 | No | No | Current |
| 11673-235-55 | 11673023555 | 1 BOTTLE in 1 CARTON (11673-235-55) > 42 TABLET, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2020-04-17 | 0000-00-00 | No | No | Current |
| 11673-235-66 | 11673023566 | 1 BOTTLE in 1 CARTON (11673-235-66) > 14 TABLET, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2018-09-27 | 0000-00-00 | No | No | Current |