mycophenolate mofetil
Generic: mycophenolate mofetil
Labeler: teva pharmaceuticals usa, inc.Drug Facts
Product Profile
Brand Name
mycophenolate mofetil
Generic Name
mycophenolate mofetil
Labeler
teva pharmaceuticals usa, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
mycophenolate mofetil 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0093-7334
Product ID
0093-7334_d924ecfe-fba4-41ad-a1c1-e8ee06d76e67
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065491
Listing Expiration
2026-12-31
Marketing Start
2009-05-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00937334
Hyphenated Format
0093-7334
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
mycophenolate mofetil (source: ndc)
Generic Name
mycophenolate mofetil (source: ndc)
Application Number
ANDA065491 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (0093-7334-01)
- 500 CAPSULE in 1 BOTTLE (0093-7334-05)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d924ecfe-fba4-41ad-a1c1-e8ee06d76e67", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["199058"], "spl_set_id": ["b414303f-e6f3-4e22-a537-96be352b59a4"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0093-7334-01)", "package_ndc": "0093-7334-01", "marketing_start_date": "20090506"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (0093-7334-05)", "package_ndc": "0093-7334-05", "marketing_start_date": "20090506"}], "brand_name": "Mycophenolate Mofetil", "product_id": "0093-7334_d924ecfe-fba4-41ad-a1c1-e8ee06d76e67", "dosage_form": "CAPSULE", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "0093-7334", "generic_name": "Mycophenolate Mofetil", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolate Mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "250 mg/1"}], "application_number": "ANDA065491", "marketing_category": "ANDA", "marketing_start_date": "20090506", "listing_expiration_date": "20261231"}