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Hydroxocobalamin
Hydroxocobalamin - 0591-2888-30 - (Hydroxocobalamin)
Drug Information of Hydroxocobalamin
| Product NDC: | 0591-2888 |
| Proprietary Name: | Hydroxocobalamin |
| Non Proprietary Name: | Hydroxocobalamin |
| Active Ingredient(s): | 1000 ug/mL & nbsp; Hydroxocobalamin |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydroxocobalamin
| Product NDC: | 0591-2888 |
| Labeler Name: | Watson Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA085998 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101112 |
Package Information of Hydroxocobalamin
| Package NDC: | 0591-2888-30 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (0591-2888-30) > 30 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Hydroxocobalamin
| NDC Code | 0591-2888-30 |
| Proprietary Name | Hydroxocobalamin |
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0591-2888-30) > 30 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 0591-2888 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydroxocobalamin |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20101112 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Laboratories, Inc. |
| Substance Name | HYDROXOCOBALAMIN ACETATE |
| Strength Number | 1000 |
| Strength Unit | ug/mL |
| Pharmaceutical Classes | Antidote [EPC] |
