← FDA Drug Approvals (Drugs@FDA)
NALOXONE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: SOLOPAK
Drug application
- FDA Application #
ANDA071672- 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
- Discontinued
- Sponsor
- SOLOPAK
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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