Package 64950-214-03

Brand: meperidine hydrochloride

Generic: meperidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 64950-214-03
Digits Only 6495021403
Product NDC 64950-214
Product ID 64950-214_0f126de5-64f4-4a0d-8caa-e97acc3a2611
Description

30 TABLET in 1 BOTTLE, PLASTIC (64950-214-03)

Marketing

Marketing Status
Marketed Since 2024-02-14
Brand meperidine hydrochloride
Generic meperidine hydrochloride
Sample Package No

Linked Drug Pages (1)

Meperidine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0f126de5-64f4-4a0d-8caa-e97acc3a2611", "openfda": {"unii": ["N8E7F7Q170"], "rxcui": ["861467"], "spl_set_id": ["792fefda-6cc4-4709-b902-fd9787fc310a"], "manufacturer_name": ["Genus Lifesciences Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (64950-214-01)", "package_ndc": "64950-214-01", "marketing_start_date": "20240214"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (64950-214-03)", "package_ndc": "64950-214-03", "marketing_start_date": "20240214"}], "brand_name": "Meperidine Hydrochloride", "product_id": "64950-214_0f126de5-64f4-4a0d-8caa-e97acc3a2611", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "64950-214", "dea_schedule": "CII", "generic_name": "Meperidine Hydrochloride", "labeler_name": "Genus Lifesciences Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meperidine Hydrochloride", "active_ingredients": [{"name": "MEPERIDINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA040893", "marketing_category": "ANDA", "marketing_start_date": "20240214", "listing_expiration_date": "20271231"}