NDC 71335-0399 – Etodolac
Etodolac 500 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0399
Product details
- Brand name
- Etodolac
- Generic name
- Etodolac
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076004
- Marketed since
- May 1, 2003
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Etodolac 500 mg/1
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0399-1 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0399-1) | Sep 5, 2024 |
| 71335-0399-2 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0399-2) | Sep 5, 2024 |
| 71335-0399-3 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0399-3) | Sep 5, 2024 |
| 71335-0399-4 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0399-4) | Sep 5, 2024 |
| 71335-0399-5 | 6 TABLET, FILM COATED in 1 BOTTLE (71335-0399-5) | Sep 5, 2024 |
| 71335-0399-6 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-0399-6) | Sep 5, 2024 |
| 71335-0399-7 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-0399-7) | Sep 5, 2024 |
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