NDC 68382-272 – Etodolac
Etodolac 500 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC68382-272
Product details
- Brand name
- Etodolac
- Generic name
- Etodolac
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA091134
- Marketed since
- February 15, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Etodolac 500 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 68382-272-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-272-01) | Feb 15, 2014 |
| 68382-272-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-272-05) | Feb 15, 2014 |
| 68382-272-10 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-272-10) | Feb 15, 2014 |
| 68382-272-14 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-272-14) | Feb 15, 2014 |
| 68382-272-77 | 100 BLISTER PACK in 1 CARTON (68382-272-77) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68382-272-30) | Feb 15, 2014 |
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