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NALOXONE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: FRESENIUS KABI USA · Approved 2024-04-02
Drug application
- FDA Application #
ANDA213573- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- NALOXONE HYDROCHLORIDE
- Generic name
- NALOXONE HYDROCHLORIDE
- Active ingredients
- NALOXONE HYDROCHLORIDE
- Dosage form
- INJECTABLE
- Route
- INJECTION
- Marketing status
- Prescription
- Sponsor
- FRESENIUS KABI USA
- Manufacturer
- Fresenius Kabi USA, LLC
- First approval
- 2024-04-02
Source
- Authoritative
- Drugs@FDA application overview
- Machine
- JSON-LD · Markdown