Mucus D ER
- Product NDC
- 56062-144
- 11-digit product format
- 560620144
- Labeler code
- 56062
- Product ID
- 56062-144_6be676e7-93bc-4b1c-914e-478b8346242a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin, pseudoephedrine hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Publix Super Markets Inc
- Application
- ANDA091071
- Marketing category
- ANDA
- Marketing start
- 2016-06-23
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE
- Active strength
- 600 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 56062-144 | MUCUS D ER (GUAIFENESIN, PSEUDOEPHEDRINE HYDROCHLORIDE) TABLET, EXTENDED RELEASE [PUBLIX SUPER MARKETS INC] | 2 | Legacy NDC | 20191126_5d2db820-28f6-4daf-8fe6-56485376eaba.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 56062-144-68 | 56062014468 | 36 BLISTER PACK in 1 CARTON (56062-144-68) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 36 blister pack | 2016-06-23 | 0000-00-00 | No | No | Current |
| 56062-144-89 | 56062014489 | 18 BLISTER PACK in 1 CARTON (56062-144-89) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 18 blister pack | 2016-06-23 | 0000-00-00 | No | No | Current |