Tussin DM
- Product NDC
- 68998-385
- 11-digit product format
- 689980385
- Labeler code
- 68998
- Product ID
- 68998-385_21f720e5-2557-4b9c-88b9-e8ceda28d6cb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dextromethorphan HBr, Guaifenesin
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Marc Glassman, Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2014-11-30
- Marketing end
- 2021-12-30
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
- Active strength
- 20 mg/10mL; mg/10mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68998-385-08 | 68998038508 | 1 BOTTLE, PLASTIC in 1 BOX (68998-385-08) > 237 mL in 1 BOTTLE, PLASTIC | 2014-11-30 | 2021-12-30 | No | No | Current |