NDC 0002-3233-01
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
- 0002-3233
- Requested NDC
- 0002-3233-01
- Package NDCs from labels
- 0002-3233-01
- Manufacturer
- National Council for Prescription Drug Programs
- Effective date
- 2013-02-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2013-02-11 | Indexing - Billing Unit |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0002-3233-01 | EA - Each | 0002-3233 | a1a40876-81b2-4d1b-ac9f-5ea7ff8f9c6e | 1 | 2013-02-11 |
| 0002-3233-30 | EA - Each | 0002-3233 | 4f610fcf-b8fb-4971-947a-5180e798ea92 | 1 | 2012-07-24 |
| 0002-3233-33 | EA - Each | 0002-3233 | 59932593-2657-4558-a765-db58b745f9a8 | 1 | 2013-02-11 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Fluoxetine | FLUOXETINE HYDROCHLORIDE | Bryant Ranch Prepack | 02283de9-6087-45f7-a9ce-3b082ce860de | 2019-02-01 | Boxed warning, Warnings, Adverse reactions | FLUOXETINE HYDROCHLORIDE |
| Fluoxetine | FLUOXETINE HYDROCHLORIDE | Vensun Pharmaceuticals, Inc. | b4f37ef1-8f5e-4318-90f1-2d8f8afb669c | 2017-09-18 | Boxed warning, Warnings, Adverse reactions | FLUOXETINE HYDROCHLORIDE |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.