NDC 53489-156 – Allopurinol
Allopurinol 100 mg/1 · Tablet · Oral
Product NDC53489-156
Product details
- Brand name
- Allopurinol
- Generic name
- Allopurinol
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA071450
- Marketed since
- January 9, 1987
- Listing expires
- December 31, 2027
- Pharmacologic class
- Xanthine Oxidase Inhibitor
Active ingredients
- Allopurinol 100 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 53489-156-01 | 100 TABLET in 1 BOTTLE, PLASTIC (53489-156-01) | Jan 9, 1987 |
| 53489-156-02 | 50 TABLET in 1 BOTTLE, PLASTIC (53489-156-02) | Jan 9, 1987 |
| 53489-156-05 | 500 TABLET in 1 BOTTLE, PLASTIC (53489-156-05) | Jan 9, 1987 |
| 53489-156-10 | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-156-10) | Jan 9, 1987 |
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