70518-4172 : Tindazole 500 mg Oral Tablet, Film Coated
NDC: | 70518-4172 |
Labeler: | Remedyrepack Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Tindazole |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA202489 |
Rev. Date: |
NDC Package Codes:
- 70518-4172-0: 8 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (70518‑4172‑0)
- 70518-4172-1: 10 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (70518‑4172‑1)
Active Ingredients:
- Tinidazole
Dosage Strength:
- 500 mg
Pharmaceutical Classes:
- Nitroimidazole Antimicrobial [EPC]
- Nitroimidazoles [CS]
Related Products:
Based on records with the same trade name.- 16571-214 Tindazole 250 mg/1 Oral Tablet, Film Coated by Pack Pharmaceuticals, LLC
- 16571-215 Tindazole 500 mg/1 Oral Tablet, Film Coated by Pack Pharmaceuticals, LLC
- 64980-426 Tindazole 250 mg Oral Tablet, Film Coated by Rising Pharmaceuticals, Inc.
- 64980-427 Tindazole 500 mg Oral Tablet, Film Coated by Rising Pharmaceuticals, Inc.
- 67296-1836 Tindazole 500 mg Oral Tablet, Film Coated by Redpharm Drug, Inc.
NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.