Package 75907-050-01
Brand: methylphenidate hydrochloride (la)
Generic: methylphenidate hydrochloridePackage Facts
Identity
Package NDC
75907-050-01
Digits Only
7590705001
Product NDC
75907-050
Description
100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (75907-050-01)
Marketing
Marketing Status
Brand
methylphenidate hydrochloride (la)
Generic
methylphenidate hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "256aeb9c-b91a-46b9-35fc-94648f5f585c", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1806177", "1806179", "1806183", "1806185", "1806195"], "spl_set_id": ["d8c14df4-ac05-d69d-9308-58a51d568329"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (75907-050-01)", "package_ndc": "75907-050-01", "marketing_start_date": "20241220"}], "brand_name": "Methylphenidate Hydrochloride (LA)", "product_id": "75907-050_256aeb9c-b91a-46b9-35fc-94648f5f585c", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "75907-050", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Dr. Reddy's Laboratories Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride (LA)", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA078458", "marketing_category": "ANDA", "marketing_start_date": "20241220", "listing_expiration_date": "20261231"}