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Folic Acid
Folic Acid - 63323-184-10 - (Folic Acid)
Drug Information of Folic Acid
| 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) |
Labeler Information of Folic Acid
| 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 Information of Folic Acid
| Package NDC: | 63323-184-10 |
| Package Description: | 1 VIAL in 1 CARTON (63323-184-10) > 10 mL in 1 VIAL |
NDC Information of Folic Acid
| NDC Code | 63323-184-10 |
| Proprietary Name | Folic Acid |
| Package Description | 1 VIAL in 1 CARTON (63323-184-10) > 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 |
