Triprolidine Hydrochloride 69367-0253
Product NDC
69367-0253- Manufacturer
- Westminster Pharmaceuticals, Llc
- Dosage Form
- Syrup
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- March 9, 2020
- Listing Expires
- December 31, 2026
- Application
- M012
Active Ingredients
| Ingredient | Strength |
|---|---|
| Triprolidine Hydrochloride | .938 mg/mL |
Packaging Options(1)
1 BOTTLE, DROPPER in 1 CARTON (69367-253-30) / 30 mL in 1 BOTTLE, DROPPER