Felodipine

Orange BookUNIISPLATC C08CA02

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerProficient Rx LP

CountryUS (United States)

ATC codeC08CA02

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 6

ndc11
7120592000
100 TABLET, FILM COATED in 1 BOTTLE (71205-920-00)
ndc11
7120592030
30 TABLET, FILM COATED in 1 BOTTLE (71205-920-30)
ndc11
7120592055
500 TABLET, FILM COATED in 1 BOTTLE (71205-920-55)
ndc11
7120592060
60 TABLET, FILM COATED in 1 BOTTLE (71205-920-60)
ndc11
7120592072
120 TABLET, FILM COATED in 1 BOTTLE (71205-920-72)
ndc11
7120592090
90 TABLET, FILM COATED in 1 BOTTLE (71205-920-90)

Annotations

UNII (FDA Substance ID)

OL961R6O2C

FELODIPINE

RxCUI 4316

Orange Book

A204800

ABABAB

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "OL961R6O2C",
    "rxcui": "4316",
    "inchikey": "RZTAMFZIAATZDJ-UHFFFAOYSA-N",
    "display_name": "FELODIPINE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "60fb803e-ccf7-46f2-b506-e157ce440f87": {
      "match": "brand_token",
      "title": "FELODIPINE TABLET, EXTENDED RELEASE [TORRENT PHARMACEUTICALS LIMITED]",
      "spl_version": "8",
      "published_date": "2026-03-02"
    }
  },
  "productid": "71205-920_06c9bc5a-7a0f-483d-bd5c-61768db340bb",
  "productndc": "71205-920",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "204800",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "2.5MG",
        "product_no": "001",
        "approval_date": "Apr 29, 2019"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "002",
        "approval_date": "Apr 29, 2019"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "003",
        "approval_date": "Apr 29, 2019"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "FELODIPINE",
  "proprietary_name": "Felodipine",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA204800",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Felodipine",
  "start_marketing_date": "20201012",
  "active_numerator_strength": "2.5"
}

Related drugs

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