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United States · US · US:70518-4616_5216f438-5ac5-eb94-e063-6394a90a5d5c

acamprosate calcium

Orange BookUNIISPLATC N07BB03

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

Identification

ManufacturerREMEDYREPACK INC.
CountryUS (United States)
ATC codeN07BB03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    7051846160
    50 POUCH in 1 BOX (70518-4616-0) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-4616-1)

Annotations

UNII (FDA Substance ID)
59375N1D0U
ACAMPROSATE CALCIUM
RxCUI 152761
Orange Book
A205995
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "59375N1D0U",
    "rxcui": "152761",
    "inchikey": "BUVGWDNTAWHSKI-UHFFFAOYSA-L",
    "display_name": "ACAMPROSATE CALCIUM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "91769a96-3182-4e38-90c3-b22c1beae398": {
      "match": "brand_token",
      "title": "ACAMPROSATE CALCIUM TABLET, DELAYED RELEASE [REMEDYREPACK INC.]",
      "spl_version": "1",
      "published_date": "2026-05-20"
    }
  },
  "productid": "70518-4616_5216f438-5ac5-eb94-e063-6394a90a5d5c",
  "productndc": "70518-4616",
  "dosage_form": "TABLET, DELAYED RELEASE",
  "orange_book": {
    "appl_no": "205995",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "333MG",
        "product_no": "001",
        "approval_date": "May 26, 2017"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ACAMPROSATE CALCIUM",
  "proprietary_name": "acamprosate calcium",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA205995",
  "marketing_category": "ANDA",
  "nonproprietary_name": "acamprosate calcium",
  "start_marketing_date": "20260423",
  "active_numerator_strength": "333"
}

Related drugs

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