NDC 0031-8744 – Robitussin Maximum Strength Severe Multi-Symptom 7 in 1 Relief Nighttime
Acetaminophen 325 mg/1; Dextromethorphan Hydrobromide 15 mg/1; Doxylamine Succinate 6.25 mg/1 · Capsule, Liquid Filled · Oral
Product NDC0031-8744
Product details
- Brand name
- Robitussin Maximum Strength Severe Multi-Symptom 7 in 1 Relief Nighttime
- Generic name
- Acetaminophen, dextromethorphan hydrobromide, and doxylamine succinate
- Labeler
- Haleon US Holdings LLC
- Dosage form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M012
- Marketed since
- July 1, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Antihistamine; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist
Active ingredients
- Acetaminophen 325 mg/1
- Dextromethorphan Hydrobromide 15 mg/1
- Doxylamine Succinate 6.25 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0031-8744-10 | 5 BLISTER PACK in 1 CARTON (0031-8744-10) / 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK | Jul 1, 2018 |