The short version
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Guaifenesin 1200 mg
Guaifenesin 1200 mg · GUAIFENESIN 1200 mg/1 · Tablet · Oral · Marksans Pharma Limited
NDC 25000-0041-12 · 500 TABLET in 1 BOTTLE · ANDA · View full market →
Medicare Part D
No Medicare Part D plan in CMS's quarterly files lists this product. That usually means it is discontinued, a repackager's listing, or a product no plan has added to its formulary.
How Part D pricing works →NADAC price per unit
No NADAC pricing on file for this NDC — NADAC covers drugs dispensed by retail community pharmacies.
Supply fragility
Not scored — fragility is computed for NADAC-priced NDCs.
Regulatory
- Application
- ANDA217780
- TE code
- —
- Approval date
- Aug 21, 2023
- Patents / exclusivity
- None on file
Shortage history
No FDA shortage reports for this drug or its presentations.
Recalls (this NDC)
No enforcement reports list this package NDC.
Manufacturers of Guaifenesin 1200 mg (Tablet)
| Labeler | Strength | First seen | Last seen |
|---|---|---|---|
| Marksans Pharma Limited | GUAIFENESIN 1200 mg/1 | Jul 15, 2026 | Sep 2, 2026 |
Roster from daily NDC Directory diffs — first/last seen dates start July 2026.
Cite this page
DrugDashboards, "Guaifenesin 1200 mg — NDC 25000-0041-12," retrieved September 3, 2026, https://drugdashboards.com/drug/25000004112.
Free to cite with attribution — see how the data is put together.