Sunmark Arthritis Pain
- Product NDC
- 70677-0108
- 11-digit product format
- 706770108
- Labeler code
- 70677
- Product ID
- 70677-0108_eeabac24-df5d-44be-b2a3-88b53441fb98
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- diclofenac sodium
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA211253
- Marketing category
- ANDA
- Marketing start
- 2020-06-03
- 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 |
|---|
| 70677-0108-1 | 70677010801 | 1 TUBE in 1 CARTON (70677-0108-1) > 100 g in 1 TUBE | 1 tube | 2020-06-03 | 0000-00-00 | No | No | Current |