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Naloxone Hydrochloride
Naloxone Hydrochloride - 0548-3369-00 - (Naloxone Hydrochloride)
Drug Information of Naloxone Hydrochloride
| Product NDC: | 0548-3369 |
| Proprietary Name: | Naloxone Hydrochloride |
| Non Proprietary Name: | Naloxone Hydrochloride |
| Active Ingredient(s): | 1 mg/mL & nbsp; Naloxone Hydrochloride |
| Administration Route(s): | PARENTERAL |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Naloxone Hydrochloride
| Product NDC: | 0548-3369 |
| Labeler Name: | Amphastar Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072076 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010601 |
Package Information of Naloxone Hydrochloride
| Package NDC: | 0548-3369-00 |
| Package Description: | 1 SYRINGE in 1 CARTON (0548-3369-00) > 2 mL in 1 SYRINGE |
NDC Information of Naloxone Hydrochloride
| NDC Code | 0548-3369-00 |
| Proprietary Name | Naloxone Hydrochloride |
| Package Description | 1 SYRINGE in 1 CARTON (0548-3369-00) > 2 mL in 1 SYRINGE |
| Product NDC | 0548-3369 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Naloxone Hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | PARENTERAL |
| Start Marketing Date | 20010601 |
| Marketing Category Name | ANDA |
| Labeler Name | Amphastar Pharmaceuticals, Inc. |
| Substance Name | NALOXONE HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
