Mucus Relief DM Extended Release Caplets
- Product NDC
- 41250-934
- 11-digit product format
- 412500934
- Labeler code
- 41250
- Product ID
- 41250-934_68927f9a-3df4-4c45-a000-948475575f5f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin, Dextromethorphan HBr
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- MEIJER, INC.
- Application
- ANDA209692
- Marketing category
- ANDA
- Marketing start
- 2018-11-05
- Marketing end
- 0000-00-00
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
- Active strength
- 60 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 |
|---|
| 41250-934-14 | 41250093414 | 14 BLISTER PACK in 1 CARTON (41250-934-14) > 1 TABLET in 1 BLISTER PACK | 14 blister pack | 2018-11-05 | 0000-00-00 | No | No | Current |
| 41250-934-28 | 41250093428 | 28 BLISTER PACK in 1 CARTON (41250-934-28) > 1 TABLET in 1 BLISTER PACK | 28 blister pack | 2018-11-05 | 0000-00-00 | No | No | Current |
| 41250-934-42 | 41250093442 | 42 BLISTER PACK in 1 CARTON (41250-934-42) > 1 TABLET in 1 BLISTER PACK | 42 blister pack | 2018-11-05 | 0000-00-00 | No | No | Current |