NALOXONE HYDROCHLORIDE
- Product NDC
- 52584-369
- 11-digit product format
- 525840369
- Labeler code
- 52584
- Product ID
- 52584-369_246eb8ce-8d10-4065-b0ad-8ed87733d592
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- naloxone hydrochloride
- Dosage form
- INJECTION
- Route
- PARENTERAL
- Labeler
- General Injectables & Vaccines, Inc.
- Application
- ANDA072076
- Marketing category
- ANDA
- Marketing start
- 2014-05-07
- Marketing end
- 2024-01-31
- Substance
- NALOXONE HYDROCHLORIDE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Opioid Antagonist [EPC], Opioid Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-369-01 | 52584036901 | 1 SYRINGE in 1 BAG (52584-369-01) > 2 mL in 1 SYRINGE | 1 syringe | 2014-05-07 | 0000-00-00 | No | No | Current |