Mucus Relief
- Product NDC
- 71141-168
- 11-digit product format
- 711410168
- Labeler code
- 71141
- Product ID
- 71141-168_ee298d18-1dcd-f7be-e053-2a95a90afcc0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- LIDL US LLC
- Application
- ANDA213420
- Marketing category
- ANDA
- Marketing start
- 2022-11-23
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 600 mg/1
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 71141-168-32 | 71141016832 | 2 PACKAGE in 1 PACKAGE (71141-168-32) > 10 TABLET, EXTENDED RELEASE in 1 PACKAGE | 2 package | 2022-11-23 | 0000-00-00 | No | No | Current |