Naloxone Hydrochloride
- Product NDC
- 71872-7219
- 11-digit product format
- 718727219
- Labeler code
- 71872
- Product ID
- 71872-7219_fa401361-8e19-c66e-e053-6394a90a30fe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naloxone Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA212455
- Marketing category
- ANDA
- Marketing start
- 2019-10-15
- Substance
- NALOXONE HYDROCHLORIDE
- Active strength
- .4 mg/mL
- Pharmacologic classes
- Opioid Antagonist [EPC], Opioid Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| F850569PQR | NALOXONE HYDROCHLORIDE | 357-08-4 | NALOXONE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7219-1 | 71872721901 | 1 VIAL, SINGLE-DOSE in 1 BAG (71872-7219-1) / 1 mL in 1 VIAL, SINGLE-DOSE | 2020-09-11 | No | No | Historical |