Mucus Relief
- Product NDC
- 59726-831
- 11-digit product format
- 597260831
- Labeler code
- 59726
- Product ID
- 59726-831_e351900b-d2e9-47a7-b921-2031955bcf46
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- ANDA207342
- Marketing category
- ANDA
- Marketing start
- 2019-03-31
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 600 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59726-831 | MUCUS RELIEF (GUAIFENESIN) TABLET [P & L DEVELOPMENT, LLC] | 5 | Legacy NDC | 20241107_28e786e9-e05c-4d11-ab79-df495908d4af.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59726-831-20 | 59726083120 | 20 BLISTER PACK in 1 CARTON (59726-831-20) > 1 TABLET in 1 BLISTER PACK | 20 blister pack | 2019-03-31 | 0000-00-00 | No | No | Current |