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Midazolam hydrochloride
Midazolam hydrochloride - 55648-762-04 - (Midazolam hydrochloride)
Drug Information of Midazolam hydrochloride
| Product NDC: | 55648-762 |
| Proprietary Name: | Midazolam hydrochloride |
| Non Proprietary Name: | Midazolam hydrochloride |
| Active Ingredient(s): | 1 mg/mL & nbsp; Midazolam hydrochloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Midazolam hydrochloride
| Product NDC: | 55648-762 |
| Labeler Name: | Wockhardt Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078141 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080530 |
Package Information of Midazolam hydrochloride
| Package NDC: | 55648-762-04 |
| Package Description: | 25 VIAL in 1 CARTON (55648-762-04) > 2 mL in 1 VIAL (55648-762-07) |
NDC Information of Midazolam hydrochloride
| NDC Code | 55648-762-04 |
| Proprietary Name | Midazolam hydrochloride |
| Package Description | 25 VIAL in 1 CARTON (55648-762-04) > 2 mL in 1 VIAL (55648-762-07) |
| Product NDC | 55648-762 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Midazolam hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20080530 |
| Marketing Category Name | ANDA |
| Labeler Name | Wockhardt Limited |
| Substance Name | MIDAZOLAM HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
