1 Vial
| Proprietary Name: Naloxone Hydrochloride |
|
| NDC Package Code: 67457-292-02 |
Strength: .4 mg/mL |
| Dosage Form: INJECTION, SOLUTION |
Route: INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Appl. No.: ANDA204997 |
Labeler Name: Mylan Institutional LLC |
| Product NDC: 67457-292 |
Nonproprietary Name: naloxone hydrochloride |
| Substance Name: NALOXONE HYDROCHLORIDE |
Product Type Name: HUMAN PRESCRIPTION DRUG |
| Start Marketing Date: 3/6/14 |
End Marketing Date: N/A |
| Market Category: ANDA |
Package Description: 10 VIAL, SINGLE-DOSE in 1 CARTON (67457-292-02) > 1 mL in 1 VIAL, SINGLE-DOSE (67457-292-00) |
| Pharm Class: Opioid Antagonist [EPC], Opioid Antagonists [MoA] |
DEA: N/A |
| Sample Package: No |
Listing Record Certified Through:: 12/31/20 |
| NDC Package Code 11-Digit Format: 67457-0292-02 |
|
| NDC Single Product Code: 67457-292-00 |
NDC Single Product Code 11-Digit Format: 67457-0292-00 |
Naloxone HCL
