NDCFind

Lofexidine 71921-0250-96

Package NDC

71921-0250-96

Product NDC: 71921-0250

Manufacturer
Florida Pharmaceutical Products, Llc
Dosage Form
Tablet, Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
August 21, 2024
Listing Expires
December 31, 2027
Application
ANDA218613
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Active Ingredients

IngredientStrength
Lofexidine Hydrochloride.18 mg/1

Selected Package

71921-0250-96Selected

1 BOTTLE in 1 CARTON (71921-250-96) / 96 TABLET, COATED in 1 BOTTLE

Other packages for this product(1)

1 BOTTLE in 1 CARTON (71921-250-36) / 36 TABLET, COATED in 1 BOTTLE