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Diazepam
Diazepam - 0409-1273-32 - (DIAZEPAM)
Drug Information of Diazepam
| Product NDC: | 0409-1273 |
| Proprietary Name: | Diazepam |
| Non Proprietary Name: | DIAZEPAM |
| Active Ingredient(s): | 5 mg/mL & nbsp; DIAZEPAM |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diazepam
| Product NDC: | 0409-1273 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072079 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19870601 |
Package Information of Diazepam
| Package NDC: | 0409-1273-32 |
| Package Description: | 100 BOX in 1 CASE (0409-1273-32) > 10 CARTRIDGE in 1 BOX > 2 mL in 1 CARTRIDGE |
NDC Information of Diazepam
| NDC Code | 0409-1273-32 |
| Proprietary Name | Diazepam |
| Package Description | 100 BOX in 1 CASE (0409-1273-32) > 10 CARTRIDGE in 1 BOX > 2 mL in 1 CARTRIDGE |
| Product NDC | 0409-1273 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DIAZEPAM |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19870601 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | DIAZEPAM |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
