NDC 50991-535 – Duraflu
Pseudoephedrine Hydrochloride 60 mg/1; Acetaminophen 325 mg/1; Dextromethorphan Hydrobromide 20 mg/1; Guaifenesin 200 mg/1 · Tablet · Oral
Product NDC50991-535
Product details
- Brand name
- Duraflu
- Generic name
- ACETAMINOPHEN, DEXTROMETHORPHAN HBr, GUAIFENESIN, PSEUDOEPHEDRINE HCl
- Labeler
- Poly Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M012
- Marketed since
- October 1, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Expectorant; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist; alpha-Adrenergic Agonist
Active ingredients
- Pseudoephedrine Hydrochloride 60 mg/1
- Acetaminophen 325 mg/1
- Dextromethorphan Hydrobromide 20 mg/1
- Guaifenesin 200 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 50991-535-01 | 100 TABLET in 1 BOTTLE (50991-535-01) | Oct 1, 2015 |
| 50991-535-02 | 6 BLISTER PACK in 1 CARTON (50991-535-02) / 2 TABLET in 1 BLISTER PACK | Oct 1, 2015 |