azathioprine sodium

Generic: azathioprine sodium

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name azathioprine sodium
Generic Name azathioprine sodium
Labeler hikma pharmaceuticals usa inc.
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

azathioprine sodium 100 mg/10mL

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-9566
Product ID 0143-9566_0d7e1bc4-3059-47a8-9331-2f37bb3c7b4e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074419
Listing Expiration 2026-12-31
Marketing Start 1995-05-01

Pharmacologic Class

Classes
nucleic acid synthesis inhibitors [moa] nucleosides [cs] purine antimetabolite [epc] purines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01439566
Hyphenated Format 0143-9566

Supplemental Identifiers

RxCUI
239983
UNII
AM94R510MS

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name azathioprine sodium (source: ndc)
Generic Name azathioprine sodium (source: ndc)
Application Number ANDA074419 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 100 mg/10mL
source: ndc
Packaging
  • 1 VIAL in 1 BOX, UNIT-DOSE (0143-9566-01) / 10 mL in 1 VIAL
source: ndc

Packages (1)

0143-9566-01 1 VIAL in 1 BOX, UNIT-DOSE (0143-9566-01) / 10 mL in 1 VIAL

Ingredients (1)

azathioprine sodium (100 mg/10mL)

Linked Drug Pages (1)

Azathioprine Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "0d7e1bc4-3059-47a8-9331-2f37bb3c7b4e", "openfda": {"unii": ["AM94R510MS"], "rxcui": ["239983"], "spl_set_id": ["9ffe79a1-ac91-4a7b-a9e3-7c84bfa9ddf0"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX, UNIT-DOSE (0143-9566-01)  / 10 mL in 1 VIAL", "package_ndc": "0143-9566-01", "marketing_start_date": "19950501"}], "brand_name": "Azathioprine Sodium", "product_id": "0143-9566_0d7e1bc4-3059-47a8-9331-2f37bb3c7b4e", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Nucleic Acid Synthesis Inhibitors [MoA]", "Nucleosides [CS]", "Purine Antimetabolite [EPC]", "Purines [CS]"], "product_ndc": "0143-9566", "generic_name": "Azathioprine Sodium", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azathioprine Sodium", "active_ingredients": [{"name": "AZATHIOPRINE SODIUM", "strength": "100 mg/10mL"}], "application_number": "ANDA074419", "marketing_category": "ANDA", "marketing_start_date": "19950501", "listing_expiration_date": "20261231"}