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Midazolam Hydrochloride
Midazolam Hydrochloride - 68094-716-62 - (Midazolam Hydrochloride)
Drug Information of Midazolam Hydrochloride
| Product NDC: | 68094-716 |
| Proprietary Name: | Midazolam Hydrochloride |
| Non Proprietary Name: | Midazolam Hydrochloride |
| Active Ingredient(s): | 10 mg/5mL & nbsp; Midazolam Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Midazolam Hydrochloride
| Product NDC: | 68094-716 |
| Labeler Name: | Precision Dose Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076379 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101011 |
Package Information of Midazolam Hydrochloride
| Package NDC: | 68094-716-62 |
| Package Description: | 3 TRAY in 1 CASE (68094-716-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (68094-716-59) |
NDC Information of Midazolam Hydrochloride
| NDC Code | 68094-716-62 |
| Proprietary Name | Midazolam Hydrochloride |
| Package Description | 3 TRAY in 1 CASE (68094-716-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (68094-716-59) |
| Product NDC | 68094-716 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Midazolam Hydrochloride |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20101011 |
| Marketing Category Name | ANDA |
| Labeler Name | Precision Dose Inc. |
| Substance Name | MIDAZOLAM HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
