NDC 72854-209 – Mucinex Nightshift Sinus Maximum Strength
Dextromethorphan Hydrobromide 10 mg/1; Acetaminophen 325 mg/1; Triprolidine Hydrochloride 1.25 mg/1 · Tablet, Coated · Oral
Product NDC72854-209
Product details
- Brand name
- Mucinex Nightshift Sinus Maximum Strength
- Generic name
- Acetaminophen, Dextromethorphan Hydrobromide, and Triprolidine Hydrochloride
- Labeler
- RB Health (US) LLC
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M012
- Marketed since
- May 1, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist
Active ingredients
- Dextromethorphan Hydrobromide 10 mg/1
- Acetaminophen 325 mg/1
- Triprolidine Hydrochloride 1.25 mg/1
Uses, dosage, side effects and warnings for Mucinex Nightshift Sinus →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 72854-209-20 | 2 BLISTER PACK in 1 CARTON (72854-209-20) / 10 TABLET, COATED in 1 BLISTER PACK | May 1, 2025 |
Other Mucinex Nightshift Sinus products
- 72854-240 Dextromethorphan Hydrobromide 10 mg/1; Phenylephrine Hydrochloride 5… · Tablet, Coated · Reckitt Benckiser LLC