Mucus Relief Extended Release
- Product NDC
- 62011-0377
- 11-digit product format
- 620110377
- Labeler code
- 62011
- Product ID
- 62011-0377_4d4b875c-890b-4d5d-8b32-b823557e8f0b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA207342
- Marketing category
- ANDA
- Marketing start
- 2018-09-30
- 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 |
|---|
| 62011-0377-1 | 62011037701 | 20 BLISTER PACK in 1 CARTON (62011-0377-1) > 1 TABLET in 1 BLISTER PACK | 20 blister pack | 2018-09-30 | 0000-00-00 | No | No | Current |