Azathioprine
- Product NDC
- 0378-1005
- 11-digit product format
- 003781005
- Labeler code
- 0378
- Product ID
- 0378-1005_6cf60af7-780e-4d86-aa30-f84dba65c02e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- azathioprine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- ANDA075568
- Marketing category
- ANDA
- Marketing start
- 2009-12-28
- Marketing end
- 2022-04-30
- Substance
- AZATHIOPRINE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Nucleic Acid Synthesis Inhibitors [MoA], Nucleosides [CS], Purine Antimetabolite [EPC], Purines [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0378-1005-01 | 00378100501 | 100 TABLET in 1 BOTTLE, PLASTIC (0378-1005-01) | 100 tablet | 2009-12-28 | 0000-00-00 | No | No | Current |