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NDC 72789-0007-06 Metronidazole 500 mg/1 Details
Metronidazole 500 mg/1
Metronidazole is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. The primary component is METRONIDAZOLE.
MedlinePlus Drug Summary
Metronidazole is used to treat infections of the reproductive system, gastrointestinal (GI) tract, skin, heart, bone, joint, lung, blood, nervous system, and other areas of the body. It is also used to treat certain sexually transmitted diseases (STDs). Metronidazole is also used to treat bacterial vaginosis (an infection caused by too much of certain types of harmful bacteria in the vagina) in women. Metronidazole is in a class of medications called nitroimidazole antimicrobials. It works by stopping the growth of bacteria. Antibiotics will not work for colds, flu, or other viral infections. Using antibiotics when they are not needed increases your risk of getting an infection later that resists antibiotic treatment.
Related Packages: 72789-0007-06Last Updated: 05/19/2024
MedLinePlus Full Drug Details: Metronidazole
Product Information
| NDC | 72789-0007 |
|---|---|
| Product ID | 72789-007_08f02263-911d-16e5-e063-6394a90a63f6 |
| Associated GPIs | 16000035000310 |
| GCN Sequence Number | 009592 |
| GCN Sequence Number Description | metronidazole TABLET 500 MG ORAL |
| HIC3 | W4E |
| HIC3 Description | ANAEROBIC ANTIPROTOZOAL-ANTIBACTERIAL AGENTS |
| GCN | 43032 |
| HICL Sequence Number | 004157 |
| HICL Sequence Number Description | METRONIDAZOLE |
| Brand/Generic | Generic |
| Proprietary Name | Metronidazole |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Metronidazole |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 500 |
| Active Ingredient Units | mg/1 |
| Substance Name | METRONIDAZOLE |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Pharmaceutical Class | Nitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA079067 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 72789-0007-06 (72789000706)
| NDC Package Code | 72789-007-06 |
|---|---|
| Billing NDC | 72789000706 |
| Package | 6 TABLET in 1 BOTTLE, PLASTIC (72789-007-06) |
| Marketing Start Date | 2023-10-30 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |