Mucus Relief DM
- Product NDC
- 68016-315
- 11-digit product format
- 680160315
- Labeler code
- 68016
- Product ID
- 68016-315_3fe0c618-31e6-4620-b6db-77caa46f7148
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin and Dextromethorphan HBr
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Chain Drug Consortium, LLC
- Application
- ANDA206941
- Marketing category
- ANDA
- Marketing start
- 2017-03-17
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE
- Active strength
- 1200 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 68016-315-14 | 68016031514 | 2 BLISTER PACK in 1 CARTON (68016-315-14) > 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 2 blister pack | 2017-03-17 | 0000-00-00 | No | No | Current |
| 68016-315-28 | 68016031528 | 4 BLISTER PACK in 1 CARTON (68016-315-28) > 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 4 blister pack | 2017-03-17 | 0000-00-00 | No | No | Current |