Naloxone Hydrochloride
- Product NDC
- 70518-2780
- 11-digit product format
- 705182780
- Labeler code
- 70518
- Product ID
- 70518-2780_d70c50cf-7e77-15be-e053-2a95a90a0713
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naloxone Hydrochloride
- Dosage form
- INJECTION
- Route
- PARENTERAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA072076
- Marketing category
- ANDA
- Marketing start
- 2020-06-11
- Marketing end
- 0000-00-00
- Substance
- NALOXONE HYDROCHLORIDE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Opioid Antagonist [EPC], Opioid Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2780-0 | 70518278000 | 10 SYRINGE in 1 BOX (70518-2780-0) > 2 mL in 1 SYRINGE (70518-2780-1) | 10 syringe | 2020-06-11 | 0000-00-00 | No | No | Current |