NDC 51655-307 – Sulfamethoxazole and Trimethoprim
Sulfamethoxazole 800 mg/1; Trimethoprim 160 mg/1 · Tablet · Oral
Product NDC51655-307
Product details
- Brand name
- Sulfamethoxazole and Trimethoprim
- Generic name
- Sulfamethoxazole and Trimethoprim
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076899
- Marketed since
- November 17, 2022
- Listing expires
- December 31, 2027
- Pharmacologic class
- Dihydrofolate Reductase Inhibitor Antibacterial; Sulfonamide Antimicrobial
Active ingredients
- Sulfamethoxazole 800 mg/1
- Trimethoprim 160 mg/1
Uses, dosage, side effects and warnings for Sulfamethoxazole and Trimethoprim →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 51655-307-20 | 20 TABLET in 1 BOTTLE, PLASTIC (51655-307-20) | Nov 17, 2022 |
| 51655-307-29 | 28 TABLET in 1 BOTTLE, PLASTIC (51655-307-29) | Feb 3, 2023 |
| 51655-307-53 | 10 TABLET in 1 BOTTLE, PLASTIC (51655-307-53) | Jan 2, 2023 |
| 51655-307-84 | 14 TABLET in 1 BOTTLE, PLASTIC (51655-307-84) | Nov 17, 2022 |
| 51655-307-87 | 6 TABLET in 1 BOTTLE, PLASTIC (51655-307-87) | Jan 12, 2023 |
Recalls mentioning this NDC
- D-0654-2025 Sep 24, 2025 · Class II
Presence of a Foreign Substance: A specific lot of auxiliary polyester coil, used in product packaging by manufacturer (Amneal Pharmaceuticals LLC) was detected with presence of a micro-organism. No…
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