NDC 71335-0126 – Etodolac
Etodolac 400 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0126
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 400 mg/1
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0126-1 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-0126-1) | Feb 20, 2018 |
| 71335-0126-2 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-0126-2) | Sep 5, 2024 |
| 71335-0126-3 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0126-3) | Nov 27, 2018 |
| 71335-0126-4 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0126-4) | Sep 5, 2024 |
| 71335-0126-5 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0126-5) | Apr 6, 2018 |
| 71335-0126-6 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0126-6) | Sep 5, 2024 |
| 71335-0126-7 | 56 TABLET, FILM COATED in 1 BOTTLE (71335-0126-7) | Feb 14, 2018 |
| 71335-0126-8 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0126-8) | Sep 5, 2024 |
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