Product NDC: | 63323-184 |
Proprietary Name: | Folic Acid |
Non Proprietary Name: | Folic Acid |
Active Ingredient(s): | 5 mg/mL & nbsp; Folic Acid |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63323-184 |
Labeler Name: | APP Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA089202 |
Marketing Category: | ANDA |
Start Marketing Date: | 20000905 |
Package NDC: | 63323-184-11 |
Package Description: | 10 VIAL in 1 TRAY (63323-184-11) > 10 mL in 1 VIAL |
NDC Code | 63323-184-11 |
Proprietary Name | Folic Acid |
Package Description | 10 VIAL in 1 TRAY (63323-184-11) > 10 mL in 1 VIAL |
Product NDC | 63323-184 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Folic Acid |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
Start Marketing Date | 20000905 |
Marketing Category Name | ANDA |
Labeler Name | APP Pharmaceuticals, LLC |
Substance Name | FOLIC ACID |
Strength Number | 5 |
Strength Unit | mg/mL |
Pharmaceutical Classes |