| Product NDC: | 0389-0486 |
| Proprietary Name: | Ascorbic Acid |
| Non Proprietary Name: | Ascorbic Acid |
| Active Ingredient(s): | 500 mg/mL & nbsp; Ascorbic Acid |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0389-0486 |
| Labeler Name: | The Torrance Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19990601 |
| Package NDC: | 0389-0486-50 |
| Package Description: | 50 VIAL, DISPENSING in 1 CARTON (0389-0486-50) > 50 mL in 1 VIAL, DISPENSING |
| NDC Code | 0389-0486-50 |
| Proprietary Name | Ascorbic Acid |
| Package Description | 50 VIAL, DISPENSING in 1 CARTON (0389-0486-50) > 50 mL in 1 VIAL, DISPENSING |
| Product NDC | 0389-0486 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ascorbic Acid |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 19990601 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | The Torrance Company |
| Substance Name | ASCORBIC ACID |
| Strength Number | 500 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |