Mucus Relief DM
- Product NDC
- 49035-825
- 11-digit product format
- 490350825
- Labeler code
- 49035
- Product ID
- 49035-825_b6f0d5d5-9371-4344-857a-42212866a507
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin, Dextromethorphan HBr
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)
- Application
- ANDA209692
- Marketing category
- ANDA
- Marketing start
- 2019-11-29
- Marketing end
- 2025-04-25
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
- Active strength
- 30 mg/1; mg/1
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
- 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 |
|---|
| 49035-825-20 | 49035082520 | 1 BOTTLE, PLASTIC in 1 BOX (49035-825-20) > 20 TABLET in 1 BOTTLE, PLASTIC | 2019-11-29 | 0000-00-00 | No | No | Current |