Mucus Relief DM MAX
- Product NDC
- 11673-834
- 11-digit product format
- 116730834
- Labeler code
- 11673
- Product ID
- 11673-834_fec1987f-aba7-443b-b55f-c43597d0e126
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dextromethorphan HBr, Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- TARGET Corporation
- Application
- ANDA209692
- Marketing category
- ANDA
- Marketing start
- 2019-01-01
- Marketing end
- 2022-12-30
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
- Active strength
- 60 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 11673-834-14 | 11673083414 | 14 BLISTER PACK in 1 CARTON (11673-834-14) > 1 TABLET in 1 BLISTER PACK | 14 blister pack | 2019-01-01 | 2022-12-30 | No | No | Current |
| 11673-834-28 | 11673083428 | 28 BLISTER PACK in 1 CARTON (11673-834-28) > 1 TABLET in 1 BLISTER PACK | 28 blister pack | 2019-01-01 | 2022-12-30 | No | No | Current |