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Naloxone Hydrochloride
Naloxone Hydrochloride - 0409-1212-01 - (NALOXONE HYDROCHLORIDE)
Drug Information of Naloxone Hydrochloride
| Product NDC: | 0409-1212 |
| Proprietary Name: | Naloxone Hydrochloride |
| Non Proprietary Name: | NALOXONE HYDROCHLORIDE |
| Active Ingredient(s): | .4 mg/mL & nbsp; NALOXONE HYDROCHLORIDE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Naloxone Hydrochloride
| Product NDC: | 0409-1212 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070254 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19870107 |
Package Information of Naloxone Hydrochloride
| Package NDC: | 0409-1212-01 |
| Package Description: | 10 AMPULE in 1 CONTAINER (0409-1212-01) > 1 mL in 1 AMPULE |
NDC Information of Naloxone Hydrochloride
| NDC Code | 0409-1212-01 |
| Proprietary Name | Naloxone Hydrochloride |
| Package Description | 10 AMPULE in 1 CONTAINER (0409-1212-01) > 1 mL in 1 AMPULE |
| Product NDC | 0409-1212 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | NALOXONE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 19870107 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | NALOXONE HYDROCHLORIDE |
| Strength Number | .4 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
