Lofexidine Hydrochloride 66993-0345-37

Package NDC

66993-0345-37

Manufacturer: Prasco Laboratories
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: August 29, 2024
Listing Expires: December 31, 2026
Application: NDA209229

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Active Ingredients

Ingredient	Strength
Lofexidine Hydrochloride	.2 mg/1

Selected Package

66993-0345-37Selected

1 BOTTLE in 1 CARTON (66993-345-37) / 36 TABLET, FILM COATED in 1 BOTTLE

Other packages for this product(1)

66993-0345-76

1 BOTTLE in 1 CARTON (66993-345-76) / 96 TABLET, FILM COATED in 1 BOTTLE

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