NDC 82922-009 - Truemed Group LLC
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
- 82922-009
- Package NDCs from labels
- 82922-009-01
- Manufacturer
- Truemed Group LLC
- Effective date
- 2022-08-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| AZATHIOPRINE - Truemed Group LLC | Truemed Group LLC | 2022-08-08 | HUMAN PRESCRIPTION DRUG LABEL |
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 |
|---|---|---|---|---|---|---|
| Azathioprine | AZATHIOPRINE | NuCare Pharmaceuticals,Inc. | 5116b22b-1460-5535-e063-6394a90acbe5 | 2026-05-05 | Boxed warning, Warnings, Adverse reactions | MRK240IY2L |
| Azathioprine | AZATHIOPRINE | REMEDYREPACK INC. | f251f372-c881-483e-8035-c6a8a6bfb4e8 | 2026-04-13 | Boxed warning, Warnings, Adverse reactions | MRK240IY2L |
| AZATHIOPRINE | AZATHIOPRINE | PD-Rx Pharmaceuticals, Inc. | d288e484-32fc-4b46-b504-d75a0fac8663 | 2026-02-16 | Boxed warning, Warnings, Adverse reactions | MRK240IY2L |
| AZATHIOPRINE | AZATHIOPRINE | AvKARE | f93d9408-7b3f-b423-e053-6294a90a31ec | 2026-01-14 | Boxed warning, Warnings, Adverse reactions | MRK240IY2L |
| AZATHIOPRINE | AZATHIOPRINE | AvKARE | d4c7d621-9642-4027-e053-2995a90a9220 | 2026-01-14 | Boxed warning, Warnings, Adverse reactions | MRK240IY2L |
| IMURAN | AZATHIOPRINE | Sebela Pharmaceuticals Inc. | 606101a0-6244-7eff-e053-2a91aa0acadd | 2025-11-08 | Boxed warning, Warnings, Adverse reactions | MRK240IY2L |
| Azathioprine | AZATHIOPRINE | Oceanside Pharmaceuticals | d72ede2c-1a9b-4717-80a7-b76a6a499936 | 2025-09-22 | Boxed warning, Warnings, Adverse reactions | MRK240IY2L |
| Azasan | AZATHIOPRINE | Salix Pharmaceuticals | 9050af7a-19c6-4670-937a-9445605de995 | 2025-09-22 | Boxed warning, Warnings, Adverse reactions | MRK240IY2L |
| Azathioprine | AZATHIOPRINE | American Health Packaging | 040d010a-b1b2-4db7-905d-8aa7f1bab0cd | 2025-05-19 | Boxed warning, Warnings, Adverse reactions | MRK240IY2L |
| Azathioprine | AZATHIOPRINE | Ascend Laboratories, LLC | bc6dc4bd-2121-4613-9d90-4a504010c98a | 2025-04-23 | Boxed warning, Warnings, Adverse reactions | MRK240IY2L |
| AZATHIOPRINE | AZATHIOPRINE | Rising Pharma Holdings, Inc. | 2ffa2fce-895d-469e-8667-b078560aec5f | 2025-02-04 | Boxed warning, Warnings, Adverse reactions | MRK240IY2L |
| Azathioprine | AZATHIOPRINE | Golden State Medical Supply, Inc. | 8429e025-b79d-dae7-e053-2a91aa0a7fe5 | 2025-01-14 | Boxed warning, Warnings, Adverse reactions | MRK240IY2L |
| Azathioprine | AZATHIOPRINE | NuCare Pharmaceuticals, Inc. | 2b9f91b9-7959-65e7-e063-6294a90a3680 | 2025-01-13 | Boxed warning, Warnings, Adverse reactions | MRK240IY2L |
| Azathioprine | AZATHIOPRINE | Zydus Lifesciences Limited | 89b272f0-ef5c-49e4-820f-fcd7ea8ef066 | 2024-11-25 | MRK240IY2L | |
| Azathioprine | AZATHIOPRINE | Zydus Lifesciences Limited | d65bc662-2ae8-4ddb-acc8-f616e72e6140 | 2024-11-25 | MRK240IY2L | |
| Azathioprine | AZATHIOPRINE | Zydus Pharmaceuticals USA Inc. | b1b0fa3e-11c3-46d0-9537-6b372c2a1b56 | 2024-08-02 | Boxed warning, Warnings, Adverse reactions | MRK240IY2L |
| ed8b578d-03cc-128a-e053-2995a90a80df | e5c21ec2-6376-471b-e053-2a95a90a3b94 | 2022-11-15 | e5c21ec2-6376-471b-e053-2a95a90a3b94 | |||
| AZATHIOPRINE | AZATHIOPRINE | Amneal Pharmaceuticals NY LLC | c49b7cc5-0eed-43b7-b7ad-cbb1b6f0cd2c | 2021-02-02 | Boxed warning, Warnings, Adverse reactions | MRK240IY2L |
| AZATHIOPRINE | AZATHIOPRINE | Aphena Pharma Solutions - Tennessee, LLC | 2f994aed-f8e7-4967-a167-b22b783b4192 | 2018-09-05 | Boxed warning, Warnings, Adverse reactions | MRK240IY2L |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.