tacrolimus

Generic: tacrolimus

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tacrolimus
Generic Name tacrolimus
Labeler major pharmaceuticals
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

tacrolimus 1 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7097
Product ID 0904-7097_0acab888-3921-40c3-a160-b4d7880a812a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090687
Listing Expiration 2026-12-31
Marketing Start 2014-08-13

Pharmacologic Class

Classes
calcineurin inhibitor immunosuppressant [epc] calcineurin inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047097
Hyphenated Format 0904-7097

Supplemental Identifiers

RxCUI
198377
UNII
WM0HAQ4WNM

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 tacrolimus (source: ndc)
Generic Name tacrolimus (source: ndc)
Application Number ANDA090687 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-7097-61) / 1 CAPSULE in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

tacrolimus (1 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0acab888-3921-40c3-a160-b4d7880a812a", "openfda": {"unii": ["WM0HAQ4WNM"], "rxcui": ["198377"], "spl_set_id": ["213f6047-f897-48a7-b78a-45d7124f2f16"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7097-61)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-7097-61", "marketing_start_date": "20140813"}], "brand_name": "Tacrolimus", "product_id": "0904-7097_0acab888-3921-40c3-a160-b4d7880a812a", "dosage_form": "CAPSULE", "pharm_class": ["Calcineurin Inhibitor Immunosuppressant [EPC]", "Calcineurin Inhibitors [MoA]"], "product_ndc": "0904-7097", "generic_name": "Tacrolimus", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tacrolimus", "active_ingredients": [{"name": "TACROLIMUS", "strength": "1 mg/1"}], "application_number": "ANDA090687", "marketing_category": "ANDA", "marketing_start_date": "20140813", "listing_expiration_date": "20261231"}