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ALSUMA
ALSUMA - 0069-0138-02 - (SUMATRIPTAN)
Drug Information of ALSUMA
| Product NDC: | 0069-0138 |
| Proprietary Name: | ALSUMA |
| Non Proprietary Name: | SUMATRIPTAN |
| Active Ingredient(s): | 6 mg/.5mL & nbsp; SUMATRIPTAN |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ALSUMA
| Product NDC: | 0069-0138 |
| Labeler Name: | Pfizer Laboratories Div Pfizer Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022041 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090831 |
Package Information of ALSUMA
| Package NDC: | 0069-0138-02 |
| Package Description: | 2 SYRINGE, GLASS in 1 CARTON (0069-0138-02) > .55 mL in 1 SYRINGE, GLASS (0069-0138-01) |
NDC Information of ALSUMA
| NDC Code | 0069-0138-02 |
| Proprietary Name | ALSUMA |
| Package Description | 2 SYRINGE, GLASS in 1 CARTON (0069-0138-02) > .55 mL in 1 SYRINGE, GLASS (0069-0138-01) |
| Product NDC | 0069-0138 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SUMATRIPTAN |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20090831 |
| Marketing Category Name | NDA |
| Labeler Name | Pfizer Laboratories Div Pfizer Inc |
| Substance Name | SUMATRIPTAN |
| Strength Number | 6 |
| Strength Unit | mg/.5mL |
| Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
