Sunmark mucus relief DM
- Product NDC
- 49348-199
- 11-digit product format
- 493480199
- Labeler code
- 49348
- Product ID
- 49348-199_96f9295e-7396-489e-89f1-af9f75043f24
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dextromethorphan HBr, Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA091070
- Marketing category
- ANDA
- Marketing start
- 2016-07-11
- 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 |
|---|
| 49348-199-46 | 49348019946 | 1 BOTTLE in 1 CARTON (49348-199-46) > 14 TABLET, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2016-07-11 | 0000-00-00 | No | No | Current |