NDC 0093-0670-06 - Gemfibrozil
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
- 0093-0670
- Requested NDC
- 0093-0670-06
- Package NDCs from labels
- 0093-0670-05, 0093-0670-06
- Manufacturer
- Teva Pharmaceuticals USA, Inc.
- Effective date
- 2017-04-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Gemfibrozil Tablets USP, 600 mg Rx only | Teva Pharmaceuticals USA, Inc. | 2017-04-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Gemfibrozil - NCS HealthCare of KY, Inc dba Vangard Labs | NCS HealthCare of KY, Inc dba Vangard Labs | 2015-01-06 | HUMAN PRESCRIPTION DRUG LABEL |
| Gemfibrozil - State of Florida DOH Central Pharmacy | State of Florida DOH Central Pharmacy | 2010-06-02 | HUMAN PRESCRIPTION DRUG LABEL |
| Gemfibrozil - Contract Pharmacy Services-PA | Contract Pharmacy Services-PA | 2010-04-05 | HUMAN PRESCRIPTION DRUG LABEL |
| GEMFIBROZIL TABLETS USP, 600 mg 0670 Rx only | Physicians Total Care, Inc. | 2010-01-26 | HUMAN PRESCRIPTION DRUG LABEL |
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2012-07-24 | Indexing - Billing Unit |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0093-0670-05 | EA - Each | 0093-0670 | 4bceda1a-6c3a-4462-b680-a38898283667 | 1 | 2012-07-24 |
| 0093-0670-06 | EA - Each | 0093-0670 | 520f7fab-9782-40ec-8b80-ec3a5f60e8fc | 1 | 2012-07-24 |
| 0093-0670-19 | EA - Each | 0093-0670 | 64a08106-fa2a-4e5a-9074-74d5e913c429 | 1 | 2012-07-24 |
| 0093-0670-93 | EA - Each | 0093-0670 | dd1d1c1a-fb90-4ce2-b527-c1cdb550844b | 1 | 2012-07-24 |
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.