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Metronidazole
Metronidazole - 50111-333-02 - (Metronidazole)
Drug Information of Metronidazole
| Product NDC: | 50111-333 |
| Proprietary Name: | Metronidazole |
| Non Proprietary Name: | Metronidazole |
| Active Ingredient(s): | 250 mg/1 & nbsp; Metronidazole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Metronidazole
| Product NDC: | 50111-333 |
| Labeler Name: | Pliva Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070027 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19900930 |
Package Information of Metronidazole
| Package NDC: | 50111-333-02 |
| Package Description: | 500 TABLET in 1 BOTTLE (50111-333-02) |
NDC Information of Metronidazole
| NDC Code | 50111-333-02 |
| Proprietary Name | Metronidazole |
| Package Description | 500 TABLET in 1 BOTTLE (50111-333-02) |
| Product NDC | 50111-333 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metronidazole |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19900930 |
| Marketing Category Name | ANDA |
| Labeler Name | Pliva Inc. |
| Substance Name | METRONIDAZOLE |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |
