Diclofenac Sodium
- Product NDC
- 55289-166
- 11-digit product format
- 552890166
- Labeler code
- 55289
- Product ID
- 55289-166_7fc11852-6ac2-43a9-e053-2a91aa0a5d9e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, In
- Application
- ANDA074376
- Marketing category
- ANDA
- Marketing start
- 1995-09-28
- Marketing end
- 0000-00-00
- Substance
- DICLOFENAC SODI
- Active strength
- 50 mg/1
- Pharmacologic classes
- Cyclooxygenase
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record