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Famotidine
Famotidine - 0069-0121-02 - (FAMOTIDINE)
Drug Information of Famotidine
| Product NDC: | 0069-0121 |
| Proprietary Name: | Famotidine |
| Non Proprietary Name: | FAMOTIDINE |
| Active Ingredient(s): | 10 mg/mL & nbsp; FAMOTIDINE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Famotidine
| Product NDC: | 0069-0121 |
| Labeler Name: | Pfizer Laboratories Div Pfizer Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078642 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110510 |
Package Information of Famotidine
| Package NDC: | 0069-0121-02 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 CARTON (0069-0121-02) > 2 mL in 1 VIAL, SINGLE-DOSE (0069-0121-01) |
NDC Information of Famotidine
| NDC Code | 0069-0121-02 |
| Proprietary Name | Famotidine |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 CARTON (0069-0121-02) > 2 mL in 1 VIAL, SINGLE-DOSE (0069-0121-01) |
| Product NDC | 0069-0121 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | FAMOTIDINE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110510 |
| Marketing Category Name | ANDA |
| Labeler Name | Pfizer Laboratories Div Pfizer Inc |
| Substance Name | FAMOTIDINE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |
