NDC 69329-323 - Diclotral Pak
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
- 69329-323
- Package NDCs from labels
- 69329-323-01
- Manufacturer
- Patchwerx Labs, Inc.
- Effective date
- 2016-03-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Diclotral Pak - Patchwerx Labs, Inc. | Patchwerx Labs, Inc. | 2016-03-11 | HUMAN PRESCRIPTION DRUG LABEL |
| diclofenac sodium delayed release tablets, capsaicin cream | Patchwerx Labs, Inc. | 2015-08-07 | HUMAN PRESCRIPTION DRUG LABEL |
| diclofenac sodium delayed release tablets, ranitidine tablets, capsaicin cream | Patchwerx Labs, Inc. | 2015-08-05 | HUMAN PRESCRIPTION DRUG LABEL |
| diclofenac sodium delayed release tablets, ranitidine tablets, capsaicin cream | Patchwerx Labs, Inc. | 2015-07-13 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 69329-323 | DICLOTRAL PAK (DICLOFENAC SODIUM, CAPSAICIN) KIT [PATCHWERX LABS, INC.] | 4 | Unmatched | 20160312_2d8f4048-14cb-7484-e054-00144ff88e88.zip |
| 69329-323 | DERMASILKRX DICLOPAK (DICLOFENAC SODIUM DELAYED RELEASE TABLETS, CAPSAICIN CREAM) KIT [PATCHWERX LABS, INC.] | 2 | Unmatched | 20150808_1cac4fd0-70cb-2bbf-e054-00144ff8d46c.zip |
| 69329-323 | DERAMSILKRX ANODYNEXA PAK (DICLOFENAC SODIUM DELAYED RELEASE TABLETS, RANITIDINE TABLETS, CAPSAICIN CREAM) KIT [PATCHWERX LABS, INC.] | 1 | Unmatched | 20150720_1b49b08b-8494-3f71-e054-00144ff88e88.zip |
| 69329-323 | DERMASILKRX DICLOPAK (DICLOFENAC SODIUM DELAYED RELEASE TABLETS, RANITIDINE TABLETS, CAPSAICIN CREAM) KIT [PATCHWERX LABS, INC.] | 1 | Unmatched | 20150805_1c948de4-dbbf-309a-e054-00144ff8d46c.zip |
DailyMed Socrata Ingredients#
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.