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daunorubicin hydrochloride
daunorubicin hydrochloride - 0703-5233-93 - (daunorubicin hydrochloride)
Drug Information of daunorubicin hydrochloride
| Product NDC: | 0703-5233 |
| Proprietary Name: | daunorubicin hydrochloride |
| Non Proprietary Name: | daunorubicin hydrochloride |
| Active Ingredient(s): | 5 mg/mL & nbsp; daunorubicin hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of daunorubicin hydrochloride
| Product NDC: | 0703-5233 |
| Labeler Name: | Teva Parenteral Medicines, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065035 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040401 |
Package Information of daunorubicin hydrochloride
| Package NDC: | 0703-5233-93 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 TRAY (0703-5233-93) > 4 mL in 1 VIAL, SINGLE-DOSE (0703-5233-91) |
NDC Information of daunorubicin hydrochloride
| NDC Code | 0703-5233-93 |
| Proprietary Name | daunorubicin hydrochloride |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 TRAY (0703-5233-93) > 4 mL in 1 VIAL, SINGLE-DOSE (0703-5233-91) |
| Product NDC | 0703-5233 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | daunorubicin hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20040401 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Parenteral Medicines, Inc. |
| Substance Name | DAUNORUBICIN HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA] |
