NDC 51672-4036 – Etodolac
Etodolac 500 mg/1 · Tablet, Film Coated · Oral
Product NDC51672-4036
Product details
- Brand name
- Etodolac
- Generic name
- Etodolac
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA075074
- Marketed since
- April 25, 2000
- Listing expires
- December 31, 2027
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Etodolac 500 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 51672-4036-1 | 100 TABLET, FILM COATED in 1 BOTTLE (51672-4036-1) | Apr 25, 2000 |
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