NDC 35916-0166 – Acetaminophen, Guaifenesin, Phenylephrine Hcl and Dextromethorphan HBr
Phenylephrine Hydrochloride 5 mg/1; Dextromethorphan Hydrobromide 10 mg/1; Acetaminophen 325 mg/1; Guaifenesin 200 mg/1 · Capsule, Liquid Filled · Oral
Product NDC35916-0166
Product details
- Brand name
- Acetaminophen, Guaifenesin, Phenylephrine Hcl and Dextromethorphan HBr
- Generic name
- Acetaminophen, Guaifenesin, Phenylephrine Hcl and Dextromethorphan HBr
- Labeler
- Softgel Healthcare Pvt Ltd
- Dosage form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M012
- Marketed since
- October 29, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Expectorant; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist; alpha-1 Adrenergic Agonist
Active ingredients
- Phenylephrine Hydrochloride 5 mg/1
- Dextromethorphan Hydrobromide 10 mg/1
- Acetaminophen 325 mg/1
- Guaifenesin 200 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 35916-0166-1 | 2 BLISTER PACK in 1 CARTON (35916-0166-1) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK | Oct 29, 2024 |