NDC 60687-630 – Nabumetone
Nabumetone 500 mg/1 · Tablet, Film Coated · Oral
Product NDC60687-630
Product details
- Brand name
- Nabumetone
- Generic name
- Nabumetone
- Labeler
- American Health Packaging
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078671
- Marketed since
- March 23, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Nabumetone 500 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 60687-630-21 | 30 BLISTER PACK in 1 CARTON (60687-630-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-630-11) | Mar 23, 2022 |
Other Nabumetone products
- 0591-3670 Nabumetone 500 mg/1 · Tablet, Film Coated · Actavis Pharma, Inc.
- 0591-3671 Nabumetone 750 mg/1 · Tablet, Film Coated · Actavis Pharma, Inc.
- 80425-0053 Nabumetone 500 mg/1 · Tablet, Film Coated · Advanced Rx of Tennessee, LLC
- 70954-784 Nabumetone 500 mg/1 · Tablet, Film Coated · ANI Pharmaceuticals, Inc.
- 70954-785 Nabumetone 750 mg/1 · Tablet, Film Coated · ANI Pharmaceuticals, Inc.
- 71335-1272 Nabumetone 750 mg/1 · Tablet, Film Coated · Bryant Ranch Prepack
- 71335-1234 Nabumetone 500 mg/1 · Tablet, Film Coated · Bryant Ranch Prepack
- 62135-146 Nabumetone 750 mg/1 · Tablet, Film Coated · Chartwell RX, LLC
- 62135-145 Nabumetone 500 mg/1 · Tablet, Film Coated · Chartwell RX, LLC
- 69097-966 Nabumetone 750 mg/1 · Tablet, Film Coated · Cipla USA Inc.
- 69097-965 Nabumetone 500 mg/1 · Tablet, Film Coated · Cipla USA Inc.
- 76282-257 Nabumetone 500 mg/1 · Tablet, Film Coated · Exelan Pharmaceuticals Inc.