Mucus Relief
- Product NDC
- 37012-728
- 11-digit product format
- 370120728
- Labeler code
- 37012
- Product ID
- 37012-728_4bc5f122-3e71-4222-9aea-d47f8e6ff456
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Shopko Stores Operating Co., LLC.
- Application
- ANDA207342
- Marketing category
- ANDA
- Marketing start
- 2018-12-31
- Marketing end
- 2024-05-31
- Substance
- GUAIFENESIN
- Active strength
- 600 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37012-728-01 | 37012072801 | 100 BLISTER PACK in 1 CARTON (37012-728-01) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2018-12-31 | 2024-05-31 | No | No | Current |