NDC 70586-2012-5 - ARTHROCEN 300 mg
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 70586-2012
- Requested NDC
- 70586-2012-5
- Package NDCs from labels
- 70586-2012-5
- Manufacturer
- Pharmin USA, LLC
- Effective date
- 2017-08-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ARTHROCEN 300 mg - Pharmin USA, LLC | Pharmin USA, LLC | 2017-08-29 | DIETARY SUPPLEMENT |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70586-2012-5 | ARTHROCEN 300 mg | 10 in 1 BLISTER PACK | CAPSULE | 10 | 1 | |
| 70586-2012-5 | ARTHROCEN 300 mg | 3 in 1 BOX | CAPSULE | 3 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70586-2012 | ARTHROCEN 300 MG (AVOCADO/SOY UNSAPONIFIABLES) CAPSULE [PHARMIN USA, LLC] | 1 | 2 package rows | 20170922_ff9dca61-2e69-4ca4-89b1-e1fac5cb1048.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.