Mucus Relief D
- Product NDC
- 0536-1137
- 11-digit product format
- 005361137
- Labeler code
- 0536
- Product ID
- 0536-1137_a0c55dff-f90c-4af5-ac04-6f09bbcb5827
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin and Pseudoephedrine Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Rugby Laboratories
- Application
- NDA021585
- Marketing category
- NDA
- Marketing start
- 2018-03-01
- 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 |
|---|
| 0536-1137 | MUCUS RELIEF D (GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE) TABLET, EXTENDED RELEASE [RUGBY LABORATORIES] | 2 | Legacy NDC | 20181102_f043ec98-6eb4-4c0c-b74c-56fdd867a520.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0536-1137-21 | 00536113721 | 1 BLISTER PACK in 1 CARTON (0536-1137-21) > 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 1 blister pack | 2018-03-01 | 0000-00-00 | No | No | Current |
| 0536-1137-36 | 00536113736 | 2 BLISTER PACK in 1 CARTON (0536-1137-36) > 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 2 blister pack | 2018-03-01 | 0000-00-00 | No | No | Current |