Details for New Drug Application (NDA): 213279
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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 213279
| Tradename: | NALOXONE HYDROCHLORIDE |
| Applicant: | Eugia Pharma |
| Ingredient: | naloxone hydrochloride |
| Patents: | 0 |
Pharmacology for NDA: 213279
| Mechanism of Action | Opioid Antagonists |
Medical Subject Heading (MeSH) Categories for 213279
Suppliers and Packaging for NDA: 213279
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| NALOXONE HYDROCHLORIDE | naloxone hydrochloride | INJECTABLE;INJECTION | 213279 | ANDA | HF Acquisition Co LLC, DBA HealthFirst | 51662-1586 | 51662-1586-1 | 1 SYRINGE in 1 BOX (51662-1586-1) / 2 mL in 1 SYRINGE |
| NALOXONE HYDROCHLORIDE | naloxone hydrochloride | INJECTABLE;INJECTION | 213279 | ANDA | HF Acquisition Co LLC, DBA HealthFirst | 51662-1586 | 51662-1586-3 | 10 POUCH in 1 CASE (51662-1586-3) / 1 BOX in 1 POUCH (51662-1586-2) / 1 SYRINGE in 1 BOX / 2 mL in 1 SYRINGE |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 1MG/ML | ||||
| Approval Date: | Jan 14, 2021 | TE: | AP | RLD: | No | ||||
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