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United States · US · US:70518-3993_3f8fc907-586d-8e31-e063-6294a90a40a0

Labetalol Hydrochloride

Orange BookUNIISPLATC C07AG01

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

Identification

ManufacturerREMEDYREPACK INC.
CountryUS (United States)
ATC codeC07AG01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 3

  • ndc11
    7051839930
    90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3993-0)
  • ndc11
    7051839931
    180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3993-1)
  • ndc11
    7051839932
    180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3993-2)

Annotations

UNII (FDA Substance ID)
1GEV3BAW9J
LABETALOL HYDROCHLORIDE
RxCUI 202693
Orange Book
A209603
ABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "1GEV3BAW9J",
    "rxcui": "202693",
    "inchikey": "WQVZLXWQESQGIF-UHFFFAOYSA-N",
    "display_name": "LABETALOL HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "d3ca153c-25b2-4506-91bd-bf9d6a4c01fe": {
      "match": "brand_token",
      "title": "LABETALOL HYDROCHLORIDE TABLET, FILM COATED [CARDINAL HEALTH 107, LLC]",
      "spl_version": "4",
      "published_date": "2026-06-01"
    }
  },
  "productid": "70518-3993_3f8fc907-586d-8e31-e063-6294a90a40a0",
  "productndc": "70518-3993",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "209603",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "001",
        "approval_date": "Jun 20, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "200MG",
        "product_no": "002",
        "approval_date": "Jun 20, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "300MG",
        "product_no": "003",
        "approval_date": "Jun 20, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "400MG",
        "product_no": "004",
        "approval_date": "Oct 18, 2024"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "LABETALOL HYDROCHLORIDE",
  "proprietary_name": "Labetalol Hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA209603",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Labetalol Hydrochloride",
  "start_marketing_date": "20240124",
  "active_numerator_strength": "200"
}

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