NDC 57344-163 – Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Guaifenesin 200 mg/1; Phenylephrine Hydrochloride 5 mg/1; Acetaminophen 325 mg/1; Dextromethorphan Hydrobromide 10 mg/1 · Tablet, Coated · Oral
Product NDC57344-163
Product details
- Brand name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
- Generic name
- ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE
- Labeler
- AAA Pharmaceutical, Inc.
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M012
- Marketed since
- August 2, 2012
- Listing expires
- December 31, 2026
- Pharmacologic class
- Expectorant; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist; alpha-1 Adrenergic Agonist
Active ingredients
- Guaifenesin 200 mg/1
- Phenylephrine Hydrochloride 5 mg/1
- Acetaminophen 325 mg/1
- Dextromethorphan Hydrobromide 10 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 57344-163-05 | 2 BLISTER PACK in 1 CARTON (57344-163-05) / 12 TABLET, COATED in 1 BLISTER PACK | Oct 28, 2015 |