Back to search
🇺🇸

United States · US · US:71335-3065_4b1e4682-4771-4ac0-afe3-4eaa71130562

Labetalol Hydrochloride

Orange BookUNIISPLATC C07AG01

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeC07AG01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 5

  • ndc11
    7133530651
    30 TABLET, FILM COATED in 1 BOTTLE (71335-3065-1)
  • ndc11
    7133530652
    90 TABLET, FILM COATED in 1 BOTTLE (71335-3065-2)
  • ndc11
    7133530653
    60 TABLET, FILM COATED in 1 BOTTLE (71335-3065-3)
  • ndc11
    7133530654
    120 TABLET, FILM COATED in 1 BOTTLE (71335-3065-4)
  • ndc11
    7133530655
    10 TABLET, FILM COATED in 1 BOTTLE (71335-3065-5)

Annotations

UNII (FDA Substance ID)
R5H8897N95
LABETALOL
RxCUI 6185
Orange Book
A075215
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "R5H8897N95",
    "rxcui": "6185",
    "inchikey": "SGUAFYQXFOLMHL-UHFFFAOYSA-N",
    "display_name": "LABETALOL",
    "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": "71335-3065_4b1e4682-4771-4ac0-afe3-4eaa71130562",
  "productndc": "71335-3065",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "075215",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "001",
        "approval_date": "Jul 29, 1999"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "200MG",
        "product_no": "002",
        "approval_date": "Jul 29, 1999"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "300MG",
        "product_no": "003",
        "approval_date": "Jul 29, 1999"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "LABETALOL",
  "proprietary_name": "Labetalol Hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA075215",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Labetalol Hydrochloride",
  "start_marketing_date": "20191122",
  "active_numerator_strength": "100"
}

Related drugs

Other records sharing ATC code C07AG01.

Access this data programmatically

Query Labetalol Hydrochloride and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.