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United States · US · US:62037-598_cf6e0dbd-317f-430e-909d-5dd9e5a59f6b

Cartia

In shortageOrange BookUNIISPLATC C05AE03

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerActavis Pharma, Inc.
CountryUS (United States)
ATC codeC05AE03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    6203759805
    500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62037-598-05)
  • ndc11
    6203759890
    90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62037-598-90)

Annotations

UNII (FDA Substance ID)
OLH94387TE
DILTIAZEM HYDROCHLORIDE
RxCUI 203211
Orange Book
A074752
AB3AB3AB3AB3
DailyMed SPL labels
1 version tracked
FDA shortage
Currently in shortage
Diltiazem Hydrochloride Injection
Raw payload (JSON)
{
  "unii": {
    "unii": "OLH94387TE",
    "rxcui": "203211",
    "inchikey": "HDRXZJPWHTXQRI-BHDTVMLSSA-N",
    "display_name": "DILTIAZEM HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "2dc2b889-8443-4f7f-83be-86c68e179804": {
      "match": "brand_token",
      "title": "CARTIA XT (DILTIAZEM HYDROCHLORIDE) CAPSULE, EXTENDED RELEASE [ACTAVIS PHARMA, INC.]",
      "spl_version": "21",
      "published_date": "2026-05-01"
    }
  },
  "productid": "62037-598_cf6e0dbd-317f-430e-909d-5dd9e5a59f6b",
  "productndc": "62037-598",
  "dosage_form": "CAPSULE, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "074752",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB3",
        "strength": "180MG",
        "product_no": "001",
        "approval_date": "Jul 9, 1998"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB3",
        "strength": "120MG",
        "product_no": "002",
        "approval_date": "Jul 9, 1998"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB3",
        "strength": "240MG",
        "product_no": "003",
        "approval_date": "Jul 9, 1998"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB3",
        "strength": "300MG",
        "product_no": "004",
        "approval_date": "Jul 9, 1998"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "DILTIAZEM HYDROCHLORIDE",
  "shortage_reason": "Diltiazem Hydrochloride Injection",
  "shortage_status": "current",
  "proprietary_name": "Cartia",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA074752",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Diltiazem Hydrochloride",
  "start_marketing_date": "19980709",
  "active_numerator_strength": "180"
}

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