Triprolidine Hydrochloride 69367-0253-30

Package NDC

69367-0253-30

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

Selected Package

69367-0253-30Selected

1 BOTTLE, DROPPER in 1 CARTON (69367-253-30) / 30 mL in 1 BOTTLE, DROPPER

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External Resources

FDA Drug Database DailyMed Label