Mucus Relief DM MAXIMUM STRENGTH
- Product NDC
- 55315-053
- 11-digit product format
- 553150053
- Labeler code
- 55315
- Product ID
- 55315-053_4ff38bf0-6b07-4d8f-a311-fc0b7474acdf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin and Dextromethorphan HBr
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Fred's, Inc.
- 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 |
|---|
| 55315-053-65 | 55315005365 | 2 BLISTER PACK in 1 CARTON (55315-053-65) > 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 2 blister pack | 2017-03-17 | 0000-00-00 | No | No | Current |