Cyproheptadine Hydrochloride 50742-0190-01

Package NDC

50742-0190-01

Manufacturer: Ingenus Pharmaceuticals Llc
Dosage Form: Tablet
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: September 23, 2015
Listing Expires: December 31, 2026
Application: ANDA205087

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Active Ingredients

Ingredient	Strength
Cyproheptadine Hydrochloride	4 mg/1

Selected Package

50742-0190-01Selected

100 TABLET in 1 BOTTLE, PLASTIC (50742-190-01)

Other packages for this product(1)

50742-0190-10

1000 TABLET in 1 BOTTLE, PLASTIC (50742-190-10)

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