NDC 69729-782 – Acetaminophen, Guaifenesin, Dextromethorphan HBr, Phenylephrine HCl
Acetaminophen 325 mg/1; Guaifenesin 200 mg/1; Dextromethorphan Hydrobromide 10 mg/1; Phenylephrine Hydrochloride 5 mg/1 · Capsule, Liquid Filled · Oral
Product NDC69729-782
Product details
- Brand name
- Acetaminophen, Guaifenesin, Dextromethorphan HBr, Phenylephrine HCl
- Generic name
- Acetaminophen, Guaifenesin, Dextromethorphan HBr, Phenylephrine HCl
- Labeler
- OPMX LLC
- Dosage form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M012
- Marketed since
- February 18, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Expectorant; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist; alpha-1 Adrenergic Agonist
Active ingredients
- Acetaminophen 325 mg/1
- Guaifenesin 200 mg/1
- Dextromethorphan Hydrobromide 10 mg/1
- Phenylephrine Hydrochloride 5 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 69729-782-10 | 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (69729-782-10) | Feb 18, 2019 |