NDC 68001-281 – Diclofenac Sodium
Diclofenac Sodium 75 mg/1 · Tablet, Delayed Release · Oral
Product NDC68001-281
Product details
- Brand name
- Diclofenac Sodium
- Generic name
- Diclofenac Sodium
- Labeler
- BluePoint Laboratories
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA077863
- Marketed since
- December 21, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Diclofenac Sodium 75 mg/1
Uses, dosage, side effects and warnings for Diclofenac Sodium →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 68001-281-00 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-281-00) | Dec 21, 2015 |
| 68001-281-03 | 500 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-281-03) | Dec 21, 2015 |
| 68001-281-06 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-281-06) | Dec 21, 2015 |
| 68001-281-08 | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-281-08) | Dec 21, 2015 |
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