Package 43598-440-01

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43598-440-01
Digits Only 4359844001
Product NDC 43598-440
Product ID 43598-440_528a86ce-1037-944a-e934-15846984dd73
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-440-01)

Marketing

Marketing Status
Discontinued 2026-09-30
Brand methylphenidate hydrochloride
Generic methylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Methylphenidate Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "528a86ce-1037-944a-e934-15846984dd73", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091155", "1091170", "1091185", "1091210"], "spl_set_id": ["7124df7e-6273-a68d-6e35-dc06122d8686"], "manufacturer_name": ["Dr.Reddys Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-440-01)", "package_ndc": "43598-440-01", "marketing_end_date": "20260930", "marketing_start_date": "20200820"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "43598-440_528a86ce-1037-944a-e934-15846984dd73", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "43598-440", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Dr.Reddys Laboratories Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "36 mg/1"}], "application_number": "ANDA213473", "marketing_category": "ANDA", "marketing_end_date": "20260930", "marketing_start_date": "20200820"}