Package 43386-931-05

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43386-931-05
Digits Only 4338693105
Product NDC 43386-931
Product ID 43386-931_69b5f215-076c-47d1-9250-1406016a5679
Description

500 mL in 1 BOTTLE (43386-931-05)

Marketing

Marketing Status
Marketed Since 2015-12-15
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": "69b5f215-076c-47d1-9250-1406016a5679", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091133", "1091341"], "spl_set_id": ["57fd619e-687d-403c-a77a-3dc3a1bab65a"], "manufacturer_name": ["Lupin Pharmaceuticals,Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BOTTLE (43386-931-05)", "package_ndc": "43386-931-05", "marketing_start_date": "20151215"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "43386-931_69b5f215-076c-47d1-9250-1406016a5679", "dosage_form": "SOLUTION", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "43386-931", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Lupin Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA204602", "marketing_category": "ANDA", "marketing_start_date": "20151215", "listing_expiration_date": "20261231"}