NDC 68071-2899-06 - Oxycodone Hydrochloride
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
- 68071-2899
- Requested NDC
- 68071-2899-06
- Package NDCs from labels
- 68071-2899-6, 68071-2899-4, 68071-2899-06
- Manufacturer
- NuCare Pharmaceuticals,Inc.
- Effective date
- 2024-09-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Oxycodone Hydrochloride - NuCare Pharmaceuticals,Inc. | NuCare Pharmaceuticals,Inc. | 2024-09-06 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68071-2899-4 | Oxycodone Hydrochloride | 4 in 1 BOTTLE, PLASTIC | TABLET | 4 | 2 | |
| 68071-2899-6 | Oxycodone Hydrochloride | 6 in 1 BOTTLE, PLASTIC | TABLET | 6 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 68071-2899 | OXYCODONE HYDROCHLORIDE TABLET [NUCARE PHARMACEUTICALS,INC.] | 2 | Current NDC, Legacy NDC, 2 package rows | 20240907_ef58f422-682e-6896-e053-2a95a90a1f2d.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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Oxycodone and Acetaminophen | OXYCODONE AND ACETAMINOPHEN | Camber Pharmaceuticals, Inc. | 2a49ee34-6f1d-4ed3-8daa-343723d2a2be | 2018-02-20 | Boxed warning, Warnings, Adverse reactions | C1ENJ2TE6C |
| OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | Ascent Pharmaceuticals Inc | de96e2be-66d9-4bcb-a133-221ad32e09f1 | 2017-07-10 | Boxed warning, Warnings, Adverse reactions | C1ENJ2TE6C |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.