NDC 68094-005-59 - 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
- 68094-005
- Requested NDC
- 68094-005-59
- Package NDCs from labels
- 68094-005-59, 68094-005-61
- Manufacturer
- Precision Dose, Inc.
- Effective date
- 2024-12-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Oxycodone Hydrochloride - Precision Dose, Inc. | Precision Dose, Inc. | 2024-12-17 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68094-005-59 | Oxycodone Hydrochloride | 10 in 1 BLISTER PACK | TABLET | 10 | 7 | |
| 68094-005-61 | Oxycodone Hydrochloride | 10 in 1 CARTON | TABLET | 10 | 7 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 68094-005-59 | EA - Each | 68094-005 | afba1f95-14ac-469f-9521-13892cd1a5cb | 1 | 2018-02-20 |
| 68094-005-61 | EA - Each | 68094-005 | b13b545b-fa08-4135-a865-c32a4abb8864 | 1 | 2017-03-06 |
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 | Asclemed USA, Inc. | 0dcb491a-54e8-486b-9575-788525a178cf | 2021-08-28 | Boxed warning, Warnings, Adverse reactions | C1ENJ2TE6C |
| Oxycodone Hydrochloride | OXYCODONE HYDROCHLORIDE | XLCare Pharmaceuticals, Inc | e5c8e72d-4ac5-4ca3-9557-6a659d4d8338 | 2021-05-28 | Boxed warning, Warnings, Adverse reactions | 1049611 1049618 C1ENJ2TE6C |
| Oxycodone and Acetaminophen | OXYCODONE AND ACETAMINOPHEN | Proficient Rx LP | dd4dbe5b-8d07-4a96-a78d-2f20da761dad | 2019-11-01 | Boxed warning, Warnings, Adverse reactions | C1ENJ2TE6C |
| Oxycodone and Acetaminophen | OXYCODONE AND ACETAMINOPHEN | Proficient Rx LP | 6253b3ae-bb52-4532-8d1f-756c0b1577c7 | 2019-11-01 | Warnings, Adverse reactions | C1ENJ2TE6C |
| Oxycodone and Acetaminophen | OXYCODONE AND ACETAMINOPHEN | Proficient Rx LP | 0233de1c-466b-4842-8604-6d879aa36a4b | 2019-11-01 | Boxed warning, Warnings, Adverse reactions | C1ENJ2TE6C |
| Oxycodone and Acetaminophen | OXYCODONE AND ACETAMINOPHEN | Proficient Rx LP | df97ea5a-51df-453b-b1b4-edc74c718ee7 | 2019-10-01 | Boxed warning, Warnings, Adverse reactions | C1ENJ2TE6C |
| 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.