Naloxone Hydrochloride
- Product NDC
- 52584-782
- 11-digit product format
- 525840782
- Labeler code
- 52584
- Product ID
- 52584-782_5faaa33f-8fb6-4a07-96be-e4c342275164
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naloxone Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- General Injectables & Vaccines, Inc
- Application
- ANDA070172
- Marketing category
- ANDA
- Marketing start
- 2010-03-01
- Marketing end
- 2023-05-01
- Substance
- NALOXONE HYDROCHLORIDE
- Active strength
- 0 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 |
|---|
| 52584-782-69 | 52584078269 | 1 BOX in 1 BAG (52584-782-69) > 1 CARTRIDGE in 1 BOX > 1 mL in 1 CARTRIDGE | 1 box | 2010-03-01 | 0000-00-00 | No | No | Current |