Diclofenac sodium
- Product NDC
- 41250-973
- 11-digit product format
- 412500973
- Labeler code
- 41250
- Product ID
- 41250-973_13ec1a5a-5f6e-4eed-97a8-0da4c1b5d6c3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diclofenac sodium
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- MEIJER, INC.
- Application
- ANDA208077
- Marketing category
- ANDA
- Marketing start
- 2021-05-03
- Marketing end
- 0000-00-00
- Substance
- DICLOFENAC SODIUM
- Active strength
- 10 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41250-973-17 | 41250097317 | 1 TUBE in 1 CARTON (41250-973-17) > 48 g in 1 TUBE | 1 tube | 2021-05-03 | 0000-00-00 | No | No | Current |