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United States · US · US:71335-0120_8dcb81bf-5383-4227-8315-13469ad46a49

lithium carbonate

Orange BookUNIISPLATC N05AN01

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN05AN01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 5

  • ndc11
    7133501201
    60 CAPSULE in 1 BOTTLE (71335-0120-1)
  • ndc11
    7133501202
    100 CAPSULE in 1 BOTTLE (71335-0120-2)
  • ndc11
    7133501203
    30 CAPSULE in 1 BOTTLE (71335-0120-3)
  • ndc11
    7133501204
    90 CAPSULE in 1 BOTTLE (71335-0120-4)
  • ndc11
    7133501205
    120 CAPSULE in 1 BOTTLE (71335-0120-5)

Annotations

UNII (FDA Substance ID)
2BMD2GNA4V
LITHIUM CARBONATE
RxCUI 42351
Orange Book
A090702
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "2BMD2GNA4V",
    "rxcui": "42351",
    "inchikey": "XGZVUEUWXADBQD-UHFFFAOYSA-L",
    "display_name": "LITHIUM CARBONATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "51b503f5-211f-a9cc-e063-6294a90a9895": {
      "match": "brand_token",
      "title": "LITHIUM CARBONATE ER (LITHIUM CARBONATE) TABLET [COUPLER LLC]",
      "spl_version": "1",
      "published_date": "2026-05-14"
    }
  },
  "productid": "71335-0120_8dcb81bf-5383-4227-8315-13469ad46a49",
  "productndc": "71335-0120",
  "dosage_form": "CAPSULE",
  "orange_book": {
    "appl_no": "090702",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "150MG",
        "product_no": "001",
        "approval_date": "Sep 25, 2009"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "300MG",
        "product_no": "002",
        "approval_date": "Sep 25, 2009"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "600MG",
        "product_no": "003",
        "approval_date": "Sep 25, 2009"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "LITHIUM CARBONATE",
  "proprietary_name": "lithium carbonate",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA090702",
  "marketing_category": "ANDA",
  "nonproprietary_name": "lithium carbonate",
  "start_marketing_date": "20091215",
  "active_numerator_strength": "300"
}

Related drugs

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