NALOXONE HYDROCHLORIDE
- Product NDC
- 71872-7215
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- NALOXONE HYDROCHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA212456
- Marketing category
- ANDA
- Substance
- NALOXONE HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 71872-7215-1 | 1 VIAL, MULTI-DOSE in 1 BAG (71872-7215-1) / 10 mL in 1 VIAL, MULTI-DOSE | 2020-06-15 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Naloxone Hydrochloride Injection, USP Opioid Antagonist Rx only | Medical Purchasing Solutions, LLC | 2023-05-03 | HUMAN PRESCRIPTION DRUG LABEL | 2 |