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Dopram
Dopram - 0641-6018-06 - (Doxapram hydrochloride)
Drug Information of Dopram
| Product NDC: | 0641-6018 |
| Proprietary Name: | Dopram |
| 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 Dopram
| Product NDC: | 0641-6018 |
| Labeler Name: | West-ward Pharmaceutical Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA014879 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19650623 |
Package Information of Dopram
| Package NDC: | 0641-6018-06 |
| Package Description: | 6 VIAL in 1 CARTON (0641-6018-06) > 20 mL in 1 VIAL (0641-6018-01) |
NDC Information of Dopram
| NDC Code | 0641-6018-06 |
| Proprietary Name | Dopram |
| Package Description | 6 VIAL in 1 CARTON (0641-6018-06) > 20 mL in 1 VIAL (0641-6018-01) |
| Product NDC | 0641-6018 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Doxapram hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19650623 |
| Marketing Category Name | NDA |
| Labeler Name | West-ward Pharmaceutical Corp. |
| Substance Name | DOXAPRAM HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Increased Medullary Respiratory Drive [PE],Respiratory Stimulant [EPC] |
