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Lithium carbonate 300 MG Extended Release Oral Tablet — RxCUI 197891

RxNorm drug concept · Semantic clinical drug
RxCUI 197891 Semantic clinical drug · SCD ● Current RxNorm concept 16 FDA products 28 package NDCs Snapshot Jul 14, 2026

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Compiled from public NLM RxNorm and FDA (openFDA NDC directory) data sources. Editorial policy

What you’re looking at: the standardized identity of one medicine, as the U.S. drug-data system sees it. Below — every FDA-listed product, package code, price benchmark, and billing code that maps to it.

🗂️ Key Facts

RxCUI197891
Official nameLithium carbonate 300 MG Extended Release Oral Tablet
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asLiCO3 300 MG Extended Release Oral Tablet
FDA products mapped16
Package NDCs mapped28
Reported Medicaid activity (SDUD)239,384 prescriptions · 52 state & territory Medicaid programs · latest period Q4 2025
RxNorm release07/06/2026
Snapshot dataJul 14, 2026

📖 Skip the Codes — Read It in Plain English.

Our pharmacist-built guide to Lithium Carbonate: what it is, how it’s used, side effects, and interactions.

📗 Our plain-language guide HelloPharmacist
  • No, lithium isn't a sedative. It's a mood stabilizer, which means it helps keep your mood more even over time. It specifically targets mania — the high, energized, and sometimes da...
  • What exactly does lithium do — is it like a sedative?
  • This is one of the most important things to understand about lithium: the amount that helps you and the amount that can seriously harm you are very close together. You can feel fin...
  • Why do I need blood tests so often? Can't my doctor just judge by how I feel?
📖 Read our full Lithium Carbonate guide →

🕸️ Concept Web — How Lithium carbonate 300 MG Extended Release Oral T... Connects

One RxCUI never lives alone. Follow the path from the raw ingredient down to the exact strength-and-form concepts FDA products carry — every stop is a real RxNorm concept with its own identifier. Hover or focus any chip for what it means.
This page's concept Lithium carbonate 300 MG Extended Release Oral Tablet RxCUI 197891

Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.

  1. Ingredients 1

    The active substance itself — no strength, form, or brand attached yet.

    • Lithium carbonate 42351
  2. Brand names 1

    The same medicine's trade names. A brand name alone says nothing about strength or form.

    • Lithobid 203321
  3. Dose forms 9

    The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.

    • Lithium carbonate Extended Release Oral Tablet 372618
    • Lithium carbonate Oral Product 1164698
    • Lithium carbonate Pill 1164699
    • Lithium carbonate Extended Release Oral Tablet [Lithobid] 370086
    • Lithobid Oral Product 1178578
    • Lithobid Pill 1178579
    • Extended Release Oral Tablet 316945
    • Oral Product 1151131
    • +1 more in this family
  4. Clinical & branded drugs 3

    Ingredient + strength + dose form. These are the concepts real FDA products actually carry.

Showing up to 8 concepts per family — 13 of 14 stored related concepts drawn.
These are official RxNorm vocabulary relationships — how concepts name and organize the same medicine. They do not establish therapeutic equivalence or substitutability: two concepts appearing in one web is never a statement that products can be swapped.

🔀 Generic ⇄ Brand Crosswalk

The same medicine has an unbranded (generic) identity and one or more brand-name identities — each with its own RxCUI. This is a naming relationship in RxNorm, not a statement that any two products are substitutable.

Generic (Clinical) Concepts

  • Lithium carbonate 300 MG SCDC · 332535
  • Lithium carbonate Extended Release Oral Tablet SCDF · 372618
  • Lithium carbonate Oral Product SCDG · 1164698
  • Lithium carbonate Pill SCDG · 1164699

Brand-Name Concepts

📦 FDA Products & Package NDCs

16 products · 28 package NDCs
28 package NDCs map to RxCUI 197891 in the current snapshot — up to 50 per page. Each linked NDC opens its full package page.
Package NDC Package Brand / generic name Labeler Marketing start
00054-0021-25 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0054-0021... Lithium Carbonate Hikma Pharmaceuticals USA Inc. 2004-10-28
00054-0021-29 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0054-0021... Lithium Carbonate Hikma Pharmaceuticals USA Inc. 2004-10-28
23155-0763-01 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (23155... Lithium carbonate Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. 2020-10-20
23155-0763-05 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (23155... Lithium carbonate Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. 2020-10-20
46708-0148-08 80 TABLET, EXTENDED RELEASE in 1 CARTON (46708-148-08) Lithium Carbonate Alembic Pharmaceuticals Limited 2017-02-21
46708-0148-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-148-30) Lithium Carbonate Alembic Pharmaceuticals Limited 2017-02-21
46708-0148-31 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-148-31) Lithium Carbonate Alembic Pharmaceuticals Limited 2017-02-21
46708-0148-91 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-148-91) Lithium Carbonate Alembic Pharmaceuticals Limited 2017-02-21
50090-1470-00 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-... Lithium Carbonate A-S Medication Solutions 2014-11-28
50090-6052-00 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-... Lithium Carbonate A-S Medication Solutions 2022-08-23
62332-0148-08 80 TABLET, EXTENDED RELEASE in 1 CARTON (62332-148-08) Lithium Carbonate Alembic Pharmaceuticals Inc. 2017-02-21
62332-0148-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-148-30) Lithium Carbonate Alembic Pharmaceuticals Inc. 2017-02-21
62332-0148-31 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-148-31) Lithium Carbonate Alembic Pharmaceuticals Inc. 2017-02-21
62332-0148-91 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-148-91) Lithium Carbonate Alembic Pharmaceuticals Inc. 2017-02-21
62559-0280-01 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62559... LITHOBID ANI Pharmaceuticals, Inc. 2014-07-01
64980-0205-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-205-01) Lithium Carbonate Rising Pharma Holdings, Inc. 2016-03-23
64980-0205-03 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-205-03) Lithium Carbonate Rising Pharma Holdings, Inc. 2016-03-23
64980-0205-05 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-205-05) Lithium Carbonate Rising Pharma Holdings, Inc. 2016-03-23
64980-0205-09 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-205-09) Lithium Carbonate Rising Pharma Holdings, Inc. 2016-03-23
67046-1575-03 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (... Lithium Carbonate Coupler LLC 2025-09-04
68084-0640-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-640-01) / 1 TAB... Lithium Carbonate American Health Packaging 2014-10-13
68462-0223-01 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462... Lithium Carbonate Glenmark Pharmaceuticals Inc., USA 2010-12-27
70518-0608-00 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-0608-0) Lithium Carbonate REMEDYREPACK INC. 2017-07-06
70518-3681-01 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3681-1) Lithium Carbonate REMEDYREPACK INC. 2026-06-19
70518-3875-00 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (... Lithium Carbonate REMEDYREPACK INC. 2023-09-26
72789-0171-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-171... Lithium Carbonate PD-Rx Pharmaceuticals, Inc. 2023-07-28
72789-0171-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-171-... Lithium Carbonate PD-Rx Pharmaceuticals, Inc. 2021-01-04
72789-0171-82 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-171... Lithium Carbonate PD-Rx Pharmaceuticals, Inc. 2023-08-23
Observed labelers: Alembic Pharmaceuticals Inc. (4) · Alembic Pharmaceuticals Limited (4) · Rising Pharma Holdings, Inc. (4) · PD-Rx Pharmaceuticals, Inc. (3) · REMEDYREPACK INC. (3) · A-S Medication Solutions (2) · +6 more — this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.

🗃️ Sources & Limits

Atlas generation902fddb9-e9c1-4004-bf4c-dba4d51037c7
openFDA export observedJul 14, 2026
RxNorm release07/06/2026
Methodology2026-07-full-catalog-v1
  • A shared RxCUI does not prove interchangeability. Products mapped to the same concept are not thereby equivalent or substitutable — equivalence is a separate, product-level determination.
  • Listing here does not establish approval or coverage. Appearing in this snapshot is a data observation, not an FDA approval status or a payer coverage decision.
  • Missing data never means zero. A silent dataset (no price, no billing code, no utilization) means no observation — not that the real-world value is zero.
  • Counts describe the mapping footprint. Product, package, and labeler counts are the FDA-listed mapping footprint in this snapshot — not sales, inventory, availability, or market share.
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.

Machine-readable JSON

Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.