Mucus D
- Product NDC
- 41250-144
- 11-digit product format
- 412500144
- Labeler code
- 41250
- Product ID
- 41250-144_9784b527-0202-4dcd-b0e0-f5ee6a92637a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin, pseudoephedrine hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Meijer Distribution Inc
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41250-144-89 | 41250014489 | 18 BLISTER PACK in 1 CARTON (41250-144-89) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 18 blister pack | 2015-12-16 | 0000-00-00 | No | No | Current |