Hydroxyzine Hydrochloride 60687-0875

Product NDC

60687-0875

Manufacturer: American Health Packaging
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: September 11, 2025
Listing Expires: December 31, 2026
Application: ANDA087871

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Active Ingredients

Ingredient	Strength
Hydroxyzine Dihydrochloride	50 mg/1

Drug Class

Antihistamine [EPC]Histamine Receptor Antagonists [MoA]

Packaging Options(1)

60687-0875-01

100 BLISTER PACK in 1 CARTON (60687-875-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-875-11)

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