simvastatin

Generic: simvastatin

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name simvastatin
Generic Name simvastatin
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

simvastatin 40 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-449
Product ID 63187-449_f5e53eb7-8199-4ca7-9cd0-8dc140c79376
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078155
Listing Expiration 2026-12-31
Marketing Start 2008-02-26

Pharmacologic Class

Established (EPC)
hmg-coa reductase inhibitor [epc]
Mechanism of Action
hydroxymethylglutaryl-coa reductase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63187449
Hyphenated Format 63187-449

Supplemental Identifiers

RxCUI
198211 312961 314231
UPC
0363187075903 0363187191900 0363187449902
UNII
AGG2FN16EV
NUI
N0000175589 N0000000121

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 simvastatin (source: ndc)
Generic Name simvastatin (source: ndc)
Application Number ANDA078155 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (63187-449-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (63187-449-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (63187-449-90)
source: ndc

Packages (3)

Ingredients (1)

simvastatin (40 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f5e53eb7-8199-4ca7-9cd0-8dc140c79376", "openfda": {"nui": ["N0000175589", "N0000000121"], "upc": ["0363187075903", "0363187191900", "0363187449902"], "unii": ["AGG2FN16EV"], "rxcui": ["198211", "312961", "314231"], "spl_set_id": ["ca760e79-5d8c-4b36-9899-0d37e8e1f24e"], "pharm_class_epc": ["HMG-CoA Reductase Inhibitor [EPC]"], "pharm_class_moa": ["Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63187-449-30)", "package_ndc": "63187-449-30", "marketing_start_date": "20181101"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63187-449-60)", "package_ndc": "63187-449-60", "marketing_start_date": "20181101"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63187-449-90)", "package_ndc": "63187-449-90", "marketing_start_date": "20181101"}], "brand_name": "simvastatin", "product_id": "63187-449_f5e53eb7-8199-4ca7-9cd0-8dc140c79376", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "63187-449", "generic_name": "simvastatin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "simvastatin", "active_ingredients": [{"name": "SIMVASTATIN", "strength": "40 mg/1"}], "application_number": "ANDA078155", "marketing_category": "ANDA", "marketing_start_date": "20080226", "listing_expiration_date": "20261231"}