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United States · US · US:71863-115_42c7a42b-6a75-69d3-e063-6294a90acc18

Betaine Anhydrous

Orange BookUNIISPLATC A16AA06

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

Identification

ManufacturerEton Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeA16AA06
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    7186311518
    180 g in 1 BOTTLE (71863-115-18)

Annotations

UNII (FDA Substance ID)
3SCV180C9W
BETAINE
RxCUI 350374
Orange Book
A210508
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "3SCV180C9W",
    "rxcui": "350374",
    "inchikey": "KWIUHFFTVRNATP-UHFFFAOYSA-N",
    "display_name": "BETAINE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "99b667fa-b00c-465b-bbed-36f317078115": {
      "match": "brand_token",
      "title": "BETAINE POWDER, FOR SOLUTION [COSETTE PHARMACEUTICALS, INC.]",
      "spl_version": "3",
      "published_date": "2026-05-21"
    }
  },
  "productid": "71863-115_42c7a42b-6a75-69d3-e063-6294a90acc18",
  "productndc": "71863-115",
  "dosage_form": "POWDER, FOR SOLUTION",
  "orange_book": {
    "appl_no": "210508",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "1GM/SCOOPFUL",
        "product_no": "001",
        "approval_date": "Jan 28, 2022"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "BETAINE",
  "proprietary_name": "Betaine Anhydrous",
  "active_ingred_unit": "g/g",
  "application_number": "ANDA210508",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Betaine Anhydrous",
  "start_marketing_date": "20220128",
  "active_numerator_strength": "1"
}

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