Naloxone Hydrochloride
- Product NDC
- 55700-985
- 11-digit product format
- 557000985
- Labeler code
- 55700
- Product ID
- 55700-985_358c3d1a-23cf-4e10-b79f-5b739f713aa9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naloxone Hydrochloride Nasal Spray
- Dosage form
- INHALANT
- Route
- NASAL
- Labeler
- Quality Care Products, LLC
- Application
- NDA208411
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2022-10-11
- Marketing end
- 0000-00-00
- Substance
- NALOXONE HYDROCHLORIDE
- Active strength
- 4 mg/.1mL
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-985-01 | 55700098501 | 2 VIAL, SINGLE-DOSE in 1 CARTON (55700-985-01) > .1 mL in 1 VIAL, SINGLE-DOSE | 2022-10-11 | 0000-00-00 | No | No | Current |