Maximum Strength Mucus Relief DM
- Product NDC
- 55910-993
- 11-digit product format
- 559100993
- Labeler code
- 55910
- Product ID
- 55910-993_4b23073c-d4c6-4c2c-9466-0b2e2e12dc12
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin and Dextromethorphan HBr
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Dolgencorp, 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 table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55910-993-05 | 55910099305 | 2 BLISTER PACK in 1 CARTON (55910-993-05) > 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 2 blister pack | 2017-03-17 | 0000-00-00 | No | No | Current |