NDC 72162-2237 – Probenecid
Probenecid 500 mg/1 · Tablet, Film Coated · Oral
Product NDC72162-2237
Product details
- Brand name
- Probenecid
- Generic name
- Probenecid
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA080966
- Marketed since
- July 29, 1976
- Listing expires
- December 31, 2026
Active ingredients
- Probenecid 500 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 72162-2237-1 | 100 TABLET, FILM COATED in 1 BOTTLE (72162-2237-1) | Jan 26, 2024 |
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