NDC 70954-005-40 - Oxybutynin Chloride
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
- 70954-005
- Requested NDC
- 70954-005-40
- Package NDCs from labels
- 70954-005-10, 70954-005-20, 70954-005-30, 70954-005-40, 70954-005-50
- Manufacturer
- Northwind Health Company, LLC
- Effective date
- 2026-01-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Oxybutynin Chloride - Northwind Health Company, LLC | Northwind Health Company, LLC | 2026-01-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Oxybutynin Chloride - VERITYRX, LLC | VERITYRX, LLC | 2025-10-31 | HUMAN PRESCRIPTION DRUG LABEL |
| Oxybutynin Chloride - Major Pharmaceuticals | Major Pharmaceuticals | 2025-09-19 | HUMAN PRESCRIPTION DRUG LABEL |
| Oxybutynin Chloride Tablets, USP Rx only | Golden State Medical Supply, Inc. | 2024-12-23 | HUMAN PRESCRIPTION DRUG LABEL |
| Oxybutynin Chloride - ANI Pharmaceuticals, Inc. | Novitium Pharma LLC | ANI Pharmaceuticals, Inc. | Novitium Pharma LLC | 2024-11-25 | Human Prescription Drug Label |
| Oxybutynin Chloride Tablets, USP 5 mg Rx only | NuCare Pharmaceuticals,Inc. | 2024-08-14 | HUMAN PRESCRIPTION DRUG LABEL |
| Oxybutynin Chloride Tablets, USP Rx only | REMEDYREPACK INC. | 2024-06-18 | HUMAN PRESCRIPTION DRUG LABEL |
| Oxybutynin Chloride - A-S Medication Solutions | A-S Medication Solutions | 2023-12-27 | Human Prescription Drug Label |
| Oxybutynin Chloride - A-S Medication Solutions | A-S Medication Solutions | 2023-12-27 | Human Prescription Drug Label |
| Oxybutynin Chloride - Denton Pharma, Inc. DBA Northwind Pharmaceuticals | Denton Pharma, Inc. DBA Northwind Pharmaceuticals | 2023-01-12 | HUMAN PRESCRIPTION DRUG LABEL |
| Oxybutynin Chloride - Bryant Ranch Prepack | Bryant Ranch Prepack | 2021-12-28 | HUMAN PRESCRIPTION DRUG LABEL |
| Oxybutynin Chloride - Denton Pharma, Inc. DBA Northwind Pharmaceuticals | Denton Pharma, Inc. DBA Northwind Pharmaceuticals | 2020-01-30 | HUMAN PRESCRIPTION DRUG LABEL |
| Oxybutynin Chloride - Marlex Pharmaceuticals Inc | Marlex Pharmaceuticals Inc | 2019-10-18 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70954-005-10 | Oxybutynin Chloride | 100 in 1 BOTTLE | TABLET | 100 | 4 | |
| 70954-005-20 | Oxybutynin Chloride | 500 in 1 BOTTLE | TABLET | 500 | 4 | |
| 70954-005-30 | Oxybutynin Chloride | 1000 in 1 BOTTLE | TABLET | 1000 | 4 | |
| 70954-005-40 | Oxybutynin Chloride | 1 in 1 BLISTER PACK | TABLET | 1 | 4 | |
| 70954-005-50 | Oxybutynin Chloride | 100 in 1 CARTON | TABLET | 100 | 4 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70954-005-10 | EA - Each | 70954-005 | 578dfbca-9e3c-4f4d-942f-e7a4d331a0dd | 1 | 2018-01-12 |
| 70954-005-20 | EA - Each | 70954-005 | ca724434-4206-4756-9065-a38e6252df49 | 1 | 2018-01-12 |
| 70954-005-30 | EA - Each | 70954-005 | ad034756-247c-496f-a21a-aae5cc3291d8 | 1 | 2018-01-12 |
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.