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Propoven
Propoven - 63323-297-30 - (PROPOFOL)
Drug Information of Propoven
| Product NDC: | 63323-297 |
| Proprietary Name: | Propoven |
| Non Proprietary Name: | PROPOFOL |
| Active Ingredient(s): | 10 mg/mL & nbsp; PROPOFOL |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Propoven
| Product NDC: | 63323-297 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
| Start Marketing Date: | 20120701 |
Package Information of Propoven
| Package NDC: | 63323-297-30 |
| Package Description: | 20 mL in 1 AMPULE (63323-297-30) |
NDC Information of Propoven
| NDC Code | 63323-297-30 |
| Proprietary Name | Propoven |
| Package Description | 20 mL in 1 AMPULE (63323-297-30) |
| Product NDC | 63323-297 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PROPOFOL |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20120701 |
| Marketing Category Name | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | PROPOFOL |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | General Anesthesia [PE],General Anesthetic [EPC] |
