naloxone hydrochloride
- Product NDC
- 43066-142
- 11-digit product format
- 430660142
- Labeler code
- 43066
- Product ID
- 43066-142_48137634-91d7-41e3-b54b-e4321d69668a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- naloxone hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Baxter Healthcare Corporation
- Application
- ANDA214785
- Marketing category
- ANDA
- Marketing start
- 2025-06-03
- Substance
- NALOXONE HYDROCHLORIDE
- Active strength
- 1 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 | 1 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F850569PQR |
| Rxcui | 1191250 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 43066-142-01 | naloxone hydrochloride | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | | 1 |
| 43066-142-01 | naloxone hydrochloride | 2 mL in 1 SYRINGE, GLASS | INJECTION, SOLUTION | 2 | | 1 |
| 43066-142-10 | naloxone hydrochloride | 10 in 1 CARTON | INJECTION, SOLUTION | 10 | | 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 |
|---|
| 43066-142-01 | 43066014201 | 1 in 1 CARTON | | | | | Historical |
| 43066-142-10 | 43066014210 | 10 CARTON in 1 CARTON (43066-142-10) / 1 SYRINGE, GLASS in 1 CARTON (43066-142-01) / 2 mL in 1 SYRINGE, GLASS | 10 carton | 2025-06-03 | No | No | Current |