Package 42806-050-30

Brand: meperidine hydrochloride

Generic: meperidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42806-050-30
Digits Only 4280605030
Product NDC 42806-050
Description

30 TABLET in 1 BOTTLE (42806-050-30)

Marketing

Marketing Status
Marketed Since 2020-01-01
Brand meperidine hydrochloride
Generic meperidine hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a2109eab-1e10-4549-adee-0700efae6f3c", "openfda": {"unii": ["N8E7F7Q170"], "rxcui": ["861455", "861467"], "spl_set_id": ["fae5cc34-5917-4445-9516-25f97ffca8db"], "manufacturer_name": ["EPIC PHARMA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42806-050-01)", "package_ndc": "42806-050-01", "marketing_start_date": "20110505"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (42806-050-30)", "package_ndc": "42806-050-30", "marketing_start_date": "20200101"}], "brand_name": "Meperidine Hydrochloride", "product_id": "42806-050_a2109eab-1e10-4549-adee-0700efae6f3c", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "42806-050", "dea_schedule": "CII", "generic_name": "Meperidine Hydrochloride", "labeler_name": "EPIC PHARMA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meperidine Hydrochloride", "active_ingredients": [{"name": "MEPERIDINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA040331", "marketing_category": "ANDA", "marketing_start_date": "20110505", "listing_expiration_date": "20261231"}