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Propofol
Propofol - 0703-2859-03 - (Propofol)
Drug Information of Propofol
| Product NDC: | 0703-2859 |
| Proprietary Name: | Propofol |
| Non Proprietary Name: | Propofol |
| Active Ingredient(s): | 10 mg/mL & nbsp; Propofol |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Propofol
| Product NDC: | 0703-2859 |
| Labeler Name: | Teva Parenteral Medicines, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075102 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070621 |
Package Information of Propofol
| Package NDC: | 0703-2859-03 |
| Package Description: | 10 VIAL, SINGLE-USE in 1 TRAY (0703-2859-03) > 100 mL in 1 VIAL, SINGLE-USE (0703-2859-01) |
NDC Information of Propofol
| NDC Code | 0703-2859-03 |
| Proprietary Name | Propofol |
| Package Description | 10 VIAL, SINGLE-USE in 1 TRAY (0703-2859-03) > 100 mL in 1 VIAL, SINGLE-USE (0703-2859-01) |
| Product NDC | 0703-2859 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Propofol |
| Dosage Form Name | INJECTION, EMULSION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20070621 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Parenteral Medicines, Inc. |
| Substance Name | PROPOFOL |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | General Anesthesia [PE],General Anesthetic [EPC] |
