meperidine hydrochloride

Generic: meperidine hydrochloride

Labeler: genus lifesciences inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name meperidine hydrochloride
Generic Name meperidine hydrochloride
Labeler genus lifesciences inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

meperidine hydrochloride 50 mg/1

Manufacturer
Genus Lifesciences Inc.

Identifiers & Regulatory

Product NDC 64950-214
Product ID 64950-214_0f126de5-64f4-4a0d-8caa-e97acc3a2611
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040893
DEA Schedule cii
Listing Expiration 2027-12-31
Marketing Start 2024-02-14

Pharmacologic Class

Classes
full opioid agonists [moa] opioid agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 64950214
Hyphenated Format 64950-214

Supplemental Identifiers

RxCUI
861467
UNII
N8E7F7Q170

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name meperidine hydrochloride (source: ndc)
Generic Name meperidine hydrochloride (source: ndc)
Application Number ANDA040893 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (64950-214-01)
  • 30 TABLET in 1 BOTTLE, PLASTIC (64950-214-03)
source: ndc

Packages (2)

64950-214-01 100 TABLET in 1 BOTTLE, PLASTIC (64950-214-01) 64950-214-03 30 TABLET in 1 BOTTLE, PLASTIC (64950-214-03)

Ingredients (1)

meperidine hydrochloride (50 mg/1)

Linked Drug Pages (1)

Meperidine Hydrochloride ndc-match (0.9)

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"}