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 |