Mucus Relief D
- Product NDC
- 0363-0144
- 11-digit product format
- 003630144
- Labeler code
- 0363
- Product ID
- 0363-0144_13e66cae-bdb8-460d-8ed8-0e40b1e4bc54
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin, pseudoephedrine hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Walgreen Company
- Application
- ANDA091071
- Marketing category
- ANDA
- Marketing start
- 2015-12-16
- 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 |
|---|
| 0363-0144 | MUCUS RELIEF D (GUAIFENESIN, PSEUDOEPHEDRINE HYDROCHLORIDE) TABLET, EXTENDED RELEASE [WALGREEN COMPANY] | 5 | Legacy NDC | 20230308_36c527af-68ee-4c60-86e6-5589f359c799.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0363-0144-68 | 00363014468 | 36 BLISTER PACK in 1 CARTON (0363-0144-68) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 36 blister pack | 2015-12-17 | 0000-00-00 | No | No | Current |
| 0363-0144-89 | 00363014489 | 18 BLISTER PACK in 1 CARTON (0363-0144-89) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 18 blister pack | 2015-12-16 | 0000-00-00 | No | No | Current |