NDC 0603-2116 – Allopurinol
Allopurinol 300 mg/1 · Tablet · Oral
Product NDC0603-2116
Product details
- Brand name
- Allopurinol
- Generic name
- Allopurinol
- Labeler
- Par Health USA, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA075798
- Marketed since
- June 27, 2003
- Listing expires
- December 31, 2027
- Pharmacologic class
- Xanthine Oxidase Inhibitor
Active ingredients
- Allopurinol 300 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 0603-2116-21 | 100 TABLET in 1 BOTTLE, PLASTIC (0603-2116-21) | Jun 27, 2003 |
| 0603-2116-28 | 500 TABLET in 1 BOTTLE, PLASTIC (0603-2116-28) | Jun 27, 2003 |
| 0603-2116-32 | 1000 TABLET in 1 BOTTLE, PLASTIC (0603-2116-32) | Jun 27, 2003 |
Recalls mentioning this NDC
- D-1405-2015 Sep 9, 2015 · Class III
Failed Tablet/Capsule Specifications; report of oversized and discolored tablets
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