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Pyridoxine Hydrochloride
Pyridoxine Hydrochloride - 63323-180-01 - (PYRIDOXINE HYDROCHLORIDE)
Drug Information of Pyridoxine Hydrochloride
| Product NDC: | 63323-180 |
| Proprietary Name: | Pyridoxine Hydrochloride |
| Non Proprietary Name: | PYRIDOXINE HYDROCHLORIDE |
| Active Ingredient(s): | 100 mg/mL & nbsp; PYRIDOXINE HYDROCHLORIDE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pyridoxine Hydrochloride
| Product NDC: | 63323-180 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA080618 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19720814 |
Package Information of Pyridoxine Hydrochloride
| Package NDC: | 63323-180-01 |
| Package Description: | 25 VIAL in 1 TRAY (63323-180-01) > 1 mL in 1 VIAL |
NDC Information of Pyridoxine Hydrochloride
| NDC Code | 63323-180-01 |
| Proprietary Name | Pyridoxine Hydrochloride |
| Package Description | 25 VIAL in 1 TRAY (63323-180-01) > 1 mL in 1 VIAL |
| Product NDC | 63323-180 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PYRIDOXINE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19720814 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | PYRIDOXINE HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
