Atorvastatin

NDC product · U.S. Food and Drug Administration (openFDA) · United States

Product NDC 70269-300
Package NDC 70269-300-00
SPL ID 6d176902-8764-49ae-96f3-dce57fba5d3a

What the source publishes

Labeler: CENTRIENT PHARMACEUTICALS INDIA PRIVATE LIMITED
Active ingredients: Atorvastatin
Form: POWDER
Administrative status: present-in-source-snapshot
Marketing status: BULK INGREDIENT
Product type: BULK INGREDIENT

Names this record is found by

Complete source data

us:fda:ndc:70269-300_6d176902-8764-49ae-96f3-dce57fba5d3a

{
  "name": "Atorvastatin",
  "splId": "6d176902-8764-49ae-96f3-dce57fba5d3a",
  "labels": [],
  "routes": [],
  "labeler": "CENTRIENT PHARMACEUTICALS INDIA PRIVATE LIMITED",
  "finished": false,
  "packaging": [
    {
      "description": "1 BAG in 1 BOX (70269-300-00)  / 25 kg in 1 BAG",
      "package_ndc": "70269-300-00",
      "identifierStatus": "well-formed",
      "marketing_start_date": "20-AUG-15"
    }
  ],
  "productId": "70269-300_6d176902-8764-49ae-96f3-dce57fba5d3a",
  "useDomain": "unknown",
  "dosageForm": "POWDER",
  "productNdc": "70269-300",
  "deaSchedule": null,
  "genericName": "Atorvastatin",
  "productType": "BULK INGREDIENT",
  "listingStatus": "present-in-source-snapshot",
  "targetSpecies": [],
  "approvalStatus": "not-established-by-ndc-listing",
  "labelAssociation": "openFDA-harmonized-set-ids; not a product-level approval match",
  "marketingEndDate": null,
  "activeIngredients": [
    {
      "name": "ATORVASTATIN CALCIUM TRIHYDRATE",
      "strength": "25 kg/25kg"
    }
  ],
  "applicationNumber": null,
  "marketingCategory": "BULK INGREDIENT",
  "stateRestrictions": {
    "status": "not-collected",
    "observations": []
  },
  "useDomainEvidence": {
    "basis": "unreviewed",
    "field": null,
    "value": null,
    "version": 1,
    "sourceId": "us.fda.ndc"
  },
  "marketingStartDate": "20150820",
  "targetSpeciesStatus": "not-reported",
  "prescriptionCategory": "unknown",
  "harmonizedIdentifiers": {},
  "listingExpirationDate": "20261231"
}

NDC Directory

U.S. Food and Drug Administration / openFDA

Retrieved: November 9, 2026
Licence: CC0 1.0
Source id: us.fda.ndc

Official source

What this source does not establish

Complete published endpoint, not a claim that FDA lists every medicine used in the US.
NDC listing, marketing category and application-number assertions are not proof of approval.
Tentative approval, discontinued products and historical submissions remain distinct.
Official document links only; linked documents have not been relicensed or mirrored.
No state restrictions, individual eligibility, or prescribing recommendations inferred.
UNII and RxNorm identifiers are source-asserted openFDA harmonization at record scope; arrays do not pair identifiers to individual products or ingredients, and are not GSID/PhPID or substitution evidence.

Read this record from your own software

The same record, with every field and its provenance, is one request away. An API key is free and works immediately.

Get your free API key Read the reference

GET /v1/drugs/record

curl -G "https://api.medifontis.com/v1/drugs/record" \
  -H "Authorization: Bearer $MEDIFONTIS_API_KEY" \
  --data-urlencode "country=us" \
  --data-urlencode "sourceId=us.fda.ndc" \
  --data-urlencode "id=us:fda:ndc:70269-300_6d176902-8764-49ae-96f3-dce57fba5d3a"