NDCFind

Cyproheptadine Hydrochloride 42708-0177-21

Package NDC

42708-0177-21

Product NDC: 42708-0177

Manufacturer
Qpharma Inc
Dosage Form
Tablet
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
January 17, 2017
Listing Expires
December 31, 2026
Application
ANDA206553
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Active Ingredients

IngredientStrength
Cyproheptadine Hydrochloride4 mg/1

Selected Package

42708-0177-21Selected

21 TABLET in 1 BOTTLE, PLASTIC (42708-177-21)