NDC 72789-102 – Cyproheptadine Hydrochloride

Cyproheptadine Hydrochloride 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72789-102

Product details

Brand name
Cyproheptadine Hydrochloride
Generic name
Cyproheptadine Hydrochloride
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206676
Marketed since
March 1, 2020
Listing expires
December 31, 2027

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
72789-102-01100 TABLET in 1 BOTTLE, PLASTIC (72789-102-01)Jul 10, 2023
72789-102-3030 TABLET in 1 BOTTLE, PLASTIC (72789-102-30)Jul 27, 2020

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