Maximum Strength Mucus Relief
- Product NDC
- 63629-8348
- 11-digit product format
- 636298348
- Labeler code
- 63629
- Product ID
- 63629-8348_eeea46d1-deb2-4381-a5dd-0a0fbd248398
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA209215
- Marketing category
- ANDA
- Marketing start
- 2019-11-06
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 1200 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8348-1 | 63629834801 | 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8348-1) | 2020-09-04 | 0000-00-00 | No | No | Current |
| 63629-8348-2 | 63629834802 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8348-2) | 2020-09-04 | 0000-00-00 | No | No | Current |