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NDC 65219-0188-10 ketamine hydrochloride 50 mg/mL Details
ketamine hydrochloride 50 mg/mL
ketamine hydrochloride is a INTRAMUSCULAR; INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Fresenius Kabi USA, LLC. The primary component is KETAMINE HYDROCHLORIDE.
Product Information
| NDC | 65219-0188 |
|---|---|
| Product ID | 65219-188_fca3eb6b-16e4-403e-9d65-71f15d9b2c45 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | ketamine hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | ketamine hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION |
| Route | INTRAMUSCULAR; INTRAVENOUS |
| Active Ingredient Strength | 50 |
| Active Ingredient Units | mg/mL |
| Substance Name | KETAMINE HYDROCHLORIDE |
| Labeler Name | Fresenius Kabi USA, LLC |
| Pharmaceutical Class | General Anesthesia [PE], General Anesthetic [EPC] |
| DEA Schedule | CIII |
| Marketing Category | ANDA |
| Application Number | ANDA215808 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 65219-0188-10 (65219018810)
| NDC Package Code | 65219-188-10 |
|---|---|
| Billing NDC | 65219018810 |
| Package | 10 VIAL in 1 TRAY (65219-188-10) / 10 mL in 1 VIAL (65219-188-01) |
| Marketing Start Date | 2023-07-10 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |