Details for New Drug Application (NDA): 213573
✉ Email this page to a colleague
The generic ingredient in NALOXONE HYDROCHLORIDE is naloxone hydrochloride; pentazocine hydrochloride. There are twelve drug master file entries for this compound. Three suppliers are listed for this compound. Additional details are available on the naloxone hydrochloride; pentazocine hydrochloride profile page.
Summary for 213573
| Tradename: | NALOXONE HYDROCHLORIDE |
| Applicant: | Fresenius Kabi Usa |
| Ingredient: | naloxone hydrochloride |
| Patents: | 0 |
Pharmacology for NDA: 213573
| Mechanism of Action | Opioid Antagonists |
Medical Subject Heading (MeSH) Categories for 213573
Suppliers and Packaging for NDA: 213573
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| NALOXONE HYDROCHLORIDE | naloxone hydrochloride | INJECTABLE;INJECTION | 213573 | ANDA | Fresenius Kabi USA, LLC | 76045-112 | 76045-112-20 | 24 SYRINGE in 1 CASE (76045-112-20) / 2 mL in 1 SYRINGE (76045-112-01) |
| NALOXONE HYDROCHLORIDE | naloxone hydrochloride | INJECTABLE;INJECTION | 213573 | ANDA | Fresenius Kabi USA, LLC | 76045-114 | 76045-114-10 | 24 SYRINGE in 1 CARTON (76045-114-10) / 1 mL in 1 SYRINGE (76045-114-01) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 0.4MG/ML | ||||
| Approval Date: | Apr 2, 2024 | TE: | AP | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 1MG/ML | ||||
| Approval Date: | Apr 2, 2024 | TE: | AP | RLD: | No | ||||
Complete Access Available with Subscription
