Cyproheptadine Hydrochloride 72789-0102-01

Package NDC

72789-0102-01

Manufacturer: Pd-Rx Pharmaceuticals, Inc.
Dosage Form: Tablet
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: March 1, 2020
Listing Expires: December 31, 2027
Application: ANDA206676

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Active Ingredients

Ingredient	Strength
Cyproheptadine Hydrochloride	4 mg/1

Selected Package

72789-0102-01Selected

100 TABLET in 1 BOTTLE, PLASTIC (72789-102-01)

Other packages for this product(1)

72789-0102-30

30 TABLET in 1 BOTTLE, PLASTIC (72789-102-30)

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