meperidine hydrochloride
Generic: meperidine hydrochloride
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
meperidine hydrochloride
Generic Name
meperidine hydrochloride
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION
Routes
Active Ingredients
meperidine hydrochloride 25 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0641-6052
Product ID
0641-6052_9566d54d-7343-4695-94ff-8b5f2d384c81
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA080445
DEA Schedule
cii
Listing Expiration
2026-12-31
Marketing Start
1975-01-22
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
06416052
Hyphenated Format
0641-6052
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA080445 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/mL
Packaging
- 25 VIAL in 1 CARTON (0641-6052-25) / 1 mL in 1 VIAL (0641-6052-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "9566d54d-7343-4695-94ff-8b5f2d384c81", "openfda": {"unii": ["N8E7F7Q170"], "rxcui": ["861476", "1665685", "1665697"], "spl_set_id": ["e0e998da-f056-4fce-be8e-ed60cf3b461b"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0641-6052-25) / 1 mL in 1 VIAL (0641-6052-01)", "package_ndc": "0641-6052-25", "marketing_start_date": "19750122"}], "brand_name": "MEPERIDINE HYDROCHLORIDE", "product_id": "0641-6052_9566d54d-7343-4695-94ff-8b5f2d384c81", "dosage_form": "INJECTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0641-6052", "dea_schedule": "CII", "generic_name": "MEPERIDINE HYDROCHLORIDE", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MEPERIDINE HYDROCHLORIDE", "active_ingredients": [{"name": "MEPERIDINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA080445", "marketing_category": "ANDA", "marketing_start_date": "19750122", "listing_expiration_date": "20261231"}