NDC 0781-9111-80 - Oxacillin
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
- 0781-9111
- Requested NDC
- 0781-9111-80
- Package NDCs from labels
- 0781-9111-80, 0781-9111-95
- Manufacturer
- Sandoz Inc
- Effective date
- 2015-09-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Oxacillin - Sandoz Inc | Sandoz Inc | 2015-09-30 | 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 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 0781-9111-95 | 2021-02-26 | C162847 | 48780-1 | 9d75b9d0-4e55-f424-e053-dadaa90a57ce | Oxacillin for Injection, USP |
| 0781-9111-95 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-4e55-f424-e053-dadaa90a57ce | Oxacillin for Injection, USP |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0781-9111-80 | EA - Each | 0781-9111 | a963cfcf-497a-4972-b39e-a6a9756d4467 | 1 | 2012-07-24 |
| 0781-9111-95 | EA - Each | 0781-9111 | 66123b5e-d6e6-46bf-bca3-422abe4b8c12 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| OXACILLIN SODIUM | ACTIVE INGREDIENT | G0V6C994Q5 | OXACILLIN INJECTION, POWDER, FOR SOLUTION [SANDOZ INC] | 14 | |
| OXACILLIN | ACTIVE MOIETY | UH95VD7V76 | OXACILLIN INJECTION, POWDER, FOR SOLUTION [SANDOZ INC] | 14 | |
| SODIUM PHOSPHATE, DIBASIC | INACTIVE INGREDIENT | GR686LBA74 | OXACILLIN INJECTION, POWDER, FOR SOLUTION [SANDOZ INC] | 14 |
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 |
|---|---|---|---|---|---|---|
| Marcs Twin Pack | SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM | Marc Glassman Inc. | 66348ee5-803a-4b78-94dd-55bc9d3543c3 | 2018-07-10 | Warnings | GR686LBA74 |
| QUALITY CHOICE SINGLE SALINE LAXATIVE | SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM | Alcyon Health, LLC. | eb499c7f-9c7b-4097-83a3-82aabffd6beb | 2017-07-12 | Warnings | GR686LBA74 |
| Pro-Enema Single Saline Laxative | SODIUM PHOSPHATE, DIBASIC AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM | Propharma Medical Supplies | e53c5eda-21da-4aed-a592-315100167cc2 | 2017-06-08 | Warnings | GR686LBA74 |
| Saline Laxative Cherry Laxative | SODIUM PHOSPHATE, DIBASIC AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM | Dolgencorp Inc. | ca3c00d9-4301-4de8-94f5-34f1bcc761ab | 2017-04-13 | Warnings | GR686LBA74 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.