NALOXONE HYDROCHLORIDE
- Product NDC
- 51662-1671
- 11-digit product format
- 516621671
- Labeler code
- 51662
- Product ID
- 51662-1671_3ba53405-5e73-c035-e063-6294a90ac0b1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- NALOXONE HYDROCHLORIDE
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- ANDA070299
- Marketing category
- ANDA
- Marketing start
- 1986-09-24
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- NALOXONE HYDROCHLORIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NALOXONE HYDROCHLORIDE | .4 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F850569PQR |
| Rxcui | 1659929 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51662-1671-1 | NALOXONE HYDROCHLORIDE | 1 mL in 1 VIAL | INJECTION | 1 | | 1 |
| 51662-1671-3 | NALOXONE HYDROCHLORIDE | 25 in 1 CARTON | INJECTION | 25 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51662-1671-1 | 51662167101 | 1 mL in 1 VIAL | 1 ml | | | | Historical |
| 51662-1671-3 | 51662167103 | 25 VIAL in 1 CARTON (51662-1671-3) / 1 mL in 1 VIAL (51662-1671-1) | 25 vial | 1986-09-24 | No | No | Current |