Mucus Relief DM Extended Release Caplets
- Product NDC
- 41250-633
- 11-digit product format
- 412500633
- Labeler code
- 41250
- Product ID
- 41250-633_2a5264b9-6543-44c5-8e01-90ceee1d2ac8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin, Dextromethorphan HBr
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- MEIJER, INC.
- Application
- ANDA209692
- Marketing category
- ANDA
- Marketing start
- 2019-01-01
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 41250-633-20 | 41250063320 | 20 BLISTER PACK in 1 CARTON (41250-633-20) > 1 TABLET in 1 BLISTER PACK | 20 blister pack | 2019-01-01 | 0000-00-00 | No | No | Current |
| 41250-633-40 | 41250063340 | 40 BLISTER PACK in 1 CARTON (41250-633-40) > 1 TABLET in 1 BLISTER PACK | 40 blister pack | 2019-01-01 | 0000-00-00 | No | No | Current |