NDC 53489-146 – Sulfamethoxazole and Trimethoprim
Sulfamethoxazole 800 mg/1; Trimethoprim 160 mg/1 · Tablet · Oral
Product NDC53489-146
Product details
- Brand name
- Sulfamethoxazole and Trimethoprim
- Generic name
- Sulfamethoxazole and Trimethoprim
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA071017
- Marketed since
- August 25, 1986
- Listing expires
- December 31, 2026
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 53489-146-01 | 100 TABLET in 1 BOTTLE, PLASTIC (53489-146-01) | Aug 25, 1986 |
| 53489-146-05 | 500 TABLET in 1 BOTTLE, PLASTIC (53489-146-05) | Aug 25, 1986 |
Recalls mentioning this NDC
- D-0802-2018 May 23, 2018 · Class II
Presence of Foreign Substance:Sun Pharma is recalling one (1) lot of Sulfamethoxazole and Trimethoprim Tablets USP, 800 mg/160 mg (500 ct.) because a foreign matter identified as polyethylene was…
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