ketalar

Generic: ketamine hydrochloride

Labeler: henry schein, inc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name ketalar
Generic Name ketamine hydrochloride
Labeler henry schein, inc
Dosage Form INJECTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

ketamine hydrochloride 10 mg/mL

Manufacturer
Henry Schein, Inc

Identifiers & Regulatory

Product NDC 0404-9880
Product ID 0404-9880_66dc4477-9189-4ff8-b778-8ceb17a50802
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA016812
DEA Schedule ciii
Listing Expiration 2026-12-31
Marketing Start 2022-01-11

Pharmacologic Class

Classes
general anesthesia [pe] general anesthetic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04049880
Hyphenated Format 0404-9880

Supplemental Identifiers

RxCUI
206967 238082
UNII
O18YUO0I83

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 ketalar (source: ndc)
Generic Name ketamine hydrochloride (source: ndc)
Application Number NDA016812 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 1 VIAL in 1 BAG (0404-9880-20) / 20 mL in 1 VIAL
source: ndc

Packages (1)

0404-9880-20 1 VIAL in 1 BAG (0404-9880-20) / 20 mL in 1 VIAL

Ingredients (1)

ketamine hydrochloride (10 mg/mL)

Linked Drug Pages (1)

KETALAR ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "66dc4477-9189-4ff8-b778-8ceb17a50802", "openfda": {"unii": ["O18YUO0I83"], "rxcui": ["206967", "238082"], "spl_set_id": ["46dab560-8ecd-4d92-8c92-6baa2310b09b"], "manufacturer_name": ["Henry Schein, Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (0404-9880-20)  / 20 mL in 1 VIAL", "package_ndc": "0404-9880-20", "marketing_start_date": "20220111"}], "brand_name": "KETALAR", "product_id": "0404-9880_66dc4477-9189-4ff8-b778-8ceb17a50802", "dosage_form": "INJECTION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "0404-9880", "dea_schedule": "CIII", "generic_name": "ketamine hydrochloride", "labeler_name": "Henry Schein, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "KETALAR", "active_ingredients": [{"name": "KETAMINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "NDA016812", "marketing_category": "NDA", "marketing_start_date": "20220111", "listing_expiration_date": "20261231"}