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Doxapram Hydrochloride
Doxapram Hydrochloride - 55390-035-01 - (Doxapram Hydrochloride)
Drug Information of Doxapram Hydrochloride
| Product NDC: | 55390-035 |
| Proprietary Name: | Doxapram Hydrochloride |
| Non Proprietary Name: | Doxapram Hydrochloride |
| Active Ingredient(s): | 20 mg/mL & nbsp; Doxapram Hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Doxapram Hydrochloride
| Product NDC: | 55390-035 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076266 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030210 |
Package Information of Doxapram Hydrochloride
| Package NDC: | 55390-035-01 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 BOX, UNIT-DOSE (55390-035-01) > 20 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Doxapram Hydrochloride
| NDC Code | 55390-035-01 |
| Proprietary Name | Doxapram Hydrochloride |
| Package Description | 1 VIAL, MULTI-DOSE in 1 BOX, UNIT-DOSE (55390-035-01) > 20 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 55390-035 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Doxapram Hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20030210 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | DOXAPRAM HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Increased Medullary Respiratory Drive [PE],Respiratory Stimulant [EPC] |
