mucus relief d
- Product NDC
- 11822-0144
- 11-digit product format
- 118220144
- Labeler code
- 11822
- Product ID
- 11822-0144_fcfaec2d-0cbe-4b88-98bd-242f46f5bd1b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin, pseudoephedrine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA091071
- Marketing category
- ANDA
- Marketing start
- 2015-12-18
- 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 |
|---|
| 11822-0144-1 | 11822014401 | 2 BLISTER PACK in 1 CARTON (11822-0144-1) > 18 TABLET in 1 BLISTER PACK | 2 blister pack | 2015-12-18 | 0000-00-00 | No | No | Current |
| 11822-0144-2 | 11822014402 | 1 BLISTER PACK in 1 CARTON (11822-0144-2) > 18 TABLET in 1 BLISTER PACK | 1 blister pack | 2015-12-18 | 0000-00-00 | No | No | Current |