NDC 0115-1757 – Cyproheptadine Hydrochloride

Cyproheptadine Hydrochloride 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0115-1757

Product details

Brand name
Cyproheptadine Hydrochloride
Generic name
Cyproheptadine Hydrochloride
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040537
Marketed since
July 29, 2015
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Cyproheptadine Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
0115-1757-01100 TABLET in 1 BOTTLE, PLASTIC (0115-1757-01)Jul 29, 2015
0115-1757-031000 TABLET in 1 BOTTLE, PLASTIC (0115-1757-03)Jul 29, 2015

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