NDC 70586-2012 - 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
- 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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.