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Midazolam Hydrochloride
Midazolam Hydrochloride - 17856-0205-1 - (Midazolam Hydrochloride)
Drug Information of Midazolam Hydrochloride
| Product NDC: | 17856-0205 |
| Proprietary Name: | Midazolam Hydrochloride |
| Non Proprietary Name: | Midazolam Hydrochloride |
| Active Ingredient(s): | 2 mg/mL & nbsp; Midazolam Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Midazolam Hydrochloride
| Product NDC: | 17856-0205 |
| Labeler Name: | Atlantic Biologicals Corps |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076058 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020705 |
Package Information of Midazolam Hydrochloride
| Package NDC: | 17856-0205-1 |
| Package Description: | 5 mL in 1 CUP (17856-0205-1) |
NDC Information of Midazolam Hydrochloride
| NDC Code | 17856-0205-1 |
| Proprietary Name | Midazolam Hydrochloride |
| Package Description | 5 mL in 1 CUP (17856-0205-1) |
| Product NDC | 17856-0205 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Midazolam Hydrochloride |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20020705 |
| Marketing Category Name | ANDA |
| Labeler Name | Atlantic Biologicals Corps |
| Substance Name | MIDAZOLAM HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
