Composition
- Active ingredients
- NALOXONE HYDROCHLORIDE 1MG/ML
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- NALOXONE HYDROCHLORIDE 4MG/SPRAY · Spray, meteredNDA208411-001 · Over the counter
- NALOXONE HYDROCHLORIDE 2MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · Spray, meteredNDA208411-002 · Discontinued
- NALOXONE HYDROCHLORIDE 1MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · InjectableNDA016636-003 · Discontinued
- NALOXONE HYDROCHLORIDE 0.4MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · InjectableNDA016636-001 · Discontinued
- NALOXONE HYDROCHLORIDE 0.02MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · InjectableNDA016636-002 · Discontinued
- NALOXONE HYDROCHLORIDE 0.4MG/ML · InjectableANDA071083-001 · Discontinued
- NALOXONE HYDROCHLORIDE 1MG/ML · InjectableANDA071311-001 · Discontinued
- NALOXONE HYDROCHLORIDE 1MG/ML · InjectableThis page
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application ANDA071084.
At a glance
- Brand name
- Narcan
- Active substance
- naloxone hydrochloride
- Route
- Injection
- Dosage form
- Injectable
- Applicant
- Bristol Myers Squibb
- Status
- Discontinued
- FDA approval
- 28 Jul 1988
- Application
- ANDA071084-001