DailyMed label

Lithium Carbonate

DailyMed label · Glenmark Pharmaceuticals Inc., USA · version 13

Key facts

Product Lithium Carbonate
Labeler Glenmark Pharmaceuticals Inc., USA
Document type HUMAN PRESCRIPTION DRUG LABEL
Active ingredients LITHIUM CARBONATE
Active ingredient UNIIs 2BMD2GNA4V
Application number 079139
Route ORAL
NDC package codes 68462-220-11, 68462-220-01, 68462-221-11, 68462-221-01, 68462-221-10, 68462-222-11, 68462-222-01
Effective date Dec 23, 2025
Set ID 63b3790f-a9b5-47f4-bae1-ddf8b43c13c1

At a glance

  • 1–9 NDC package codes
  • 1–9 Active ingredients
  • 1–9 Manufacturing establishments listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.

Source: U.S. National Library of Medicine (NLM), DailyMed · Source date:

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