Naloxone Hydrochloride
- Product NDC
- 17478-041
- 11-digit product format
- 174780041
- Labeler code
- 17478
- Product ID
- 17478-041_c169f27e-a661-4482-8303-0a0d4d811655
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naloxone Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Akorn
- Application
- ANDA208871
- Marketing category
- ANDA
- Marketing start
- 2017-02-28
- Marketing end
- 0000-00-00
- Substance
- NALOXONE HYDROCHLORIDE
- Active strength
- 0 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17478-041-01 | Naloxone Hydrochloride | 1 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 1 | | 12 |
| 17478-041-01 | Naloxone Hydrochloride | 10 in 1 CARTON | INJECTION, SOLUTION | 10 | | 12 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17478-041 | NALOXONE HYDROCHLORIDE INJECTION, SOLUTION [AKORN] | 12 | Legacy NDC, 2 package rows | 20220915_747e602c-93f9-4723-a899-4c1c55c35ef8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17478-041-01 | 17478004101 | 10 VIAL, SINGLE-DOSE in 1 CARTON (17478-041-01) > 1 mL in 1 VIAL, SINGLE-DOSE | 2017-02-28 | 0000-00-00 | No | No | Current |