lithium carbonate

Orange BookUNIISPLATC N05AN01

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerCamber Pharmaceuticals, Inc.

CountryUS (United States)

ATC codeN05AN01

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
3172254601
100 CAPSULE in 1 BOTTLE (31722-546-01)
ndc11
3172254605
500 CAPSULE in 1 BOTTLE (31722-546-05)
ndc11
3172254610
1000 CAPSULE in 1 BOTTLE (31722-546-10)
ndc11
3172254630
30 CAPSULE in 1 BOTTLE (31722-546-30)

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": "31722-546_f0c7a72e-0f38-6613-e053-2a95a90a612c",
  "productndc": "31722-546",
  "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": "600"
}

Related drugs

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