FDA.reportPublic FDA data

NDC 46708-014-30 - Lithium Carbonate

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
46708-014
Requested NDC
46708-014-30
Package NDCs from labels
46708-014-30, 46708-014-31, 46708-014-71, 46708-014-91
Manufacturer
Alembic Limited
Effective date
2009-01-27
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Lithium Carbonate - Alembic LimitedAlembic Limited2009-01-27HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
46708-014-30Lithium Carbonate30 in 1 BOTTLECAPSULE301
46708-014-31Lithium Carbonate100 in 1 BOTTLECAPSULE1001
46708-014-71Lithium Carbonate500 in 1 BOTTLECAPSULE5001
46708-014-91Lithium Carbonate1000 in 1 BOTTLECAPSULE10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
46708-014LITHIUM CARBONATE CAPSULE [ALEMBIC LIMITED]14 package rows20090212_083ca85f-a450-4fe9-973e-47a13cd18dd1.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
lithium carbonateACTIVE INGREDIENT2BMD2GNA4VLITHIUM CARBONATE CAPSULE [ALEMBIC LIMITED]1
lithium cationACTIVE MOIETY8H8Z5UER66LITHIUM CARBONATE CAPSULE [ALEMBIC LIMITED]1
black iron oxideINACTIVE INGREDIENTLITHIUM CARBONATE CAPSULE [ALEMBIC LIMITED]1
D&C Yellow No. 10INACTIVE INGREDIENTLITHIUM CARBONATE CAPSULE [ALEMBIC LIMITED]1
FD&C Red No. 40INACTIVE INGREDIENTLITHIUM CARBONATE CAPSULE [ALEMBIC LIMITED]1
FD&C Yellow No. 6INACTIVE INGREDIENTLITHIUM CARBONATE CAPSULE [ALEMBIC LIMITED]1
gelatinINACTIVE INGREDIENT2G86QN327LLITHIUM CARBONATE CAPSULE [ALEMBIC LIMITED]1
talcINACTIVE INGREDIENT7SEV7J4R1ULITHIUM CARBONATE CAPSULE [ALEMBIC LIMITED]1
titanium dioxideINACTIVE INGREDIENT15FIX9V2JPLITHIUM CARBONATE CAPSULE [ALEMBIC LIMITED]1

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 2 · 25 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Lithium CarbonateLITHIUM CARBONATEHikma Pharmaceuticals USA Inc.b839ff4b-f62d-41ab-a823-550a756d58ec2026-08-16Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311355
rxcui: 197893
rxcui: 197889
lithium carbonateLITHIUM CARBONATECoupler LLC582697c1-063f-366f-e063-6294a90a8d1b2026-08-03Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311355
Lithium CarbonateLITHIUM CARBONATEREMEDYREPACK INC.803eab29-0d0a-4df0-b504-bcd85ec01ead2026-07-21Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 197893
Lithium CarbonateLITHIUM CARBONATEREMEDYREPACK INC.1c320bff-b4d5-42f2-b2b5-238564fe95892026-07-15Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 197889
Lithium CarbonateLITHIUM CARBONATEREMEDYREPACK INC.05312159-3d8a-45e0-99cb-b83a7b200cd32026-07-06Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311355
Lithium CarbonateLITHIUM CARBONATEREMEDYREPACK INC.b074ca9f-66b2-4e83-b67d-cb317b46411b2026-06-15Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 197893
Lithium CarbonateLITHIUM CARBONATECardinal Health 107, LLC0e6b0a2d-b79c-44d8-b785-5267df9e8f722026-06-04Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 197889
Lithium CarbonateLITHIUM CARBONATEBryant Ranch Prepack1a62d5ae-a4a3-4b10-8281-feba134bbe3a2026-06-03Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 197889
Lithium CarbonateLITHIUM CARBONATEAmerican Health Packaging049902a9-3af1-4863-994e-15f36e7a97932026-05-26Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 197893
rxcui: 197889
Lithium CarbonateLITHIUM CARBONATECoupler LLC5102eb69-4872-53fb-e063-6394a90a82752026-05-04Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311355
lithium carbonateLITHIUM CARBONATEREMEDYREPACK INC.01c4facd-ed79-4078-ba33-2044de372d0f2026-04-27Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311355
Lithium CarbonateLITHIUM CARBONATEREMEDYREPACK INC.57faf0b0-4380-4bbf-8de7-c3f9d74fc4102026-04-13Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311355
Lithium CarbonateLITHIUM CARBONATEGlenmark Pharmaceuticals Inc., USA63b3790f-a9b5-47f4-bae1-ddf8b43c13c12025-12-23Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311355
rxcui: 197893
rxcui: 197889
Lithium CarbonateLITHIUM CARBONATEPD-Rx Pharmaceuticals, Inc.16ebe1f9-501d-468b-a37d-f6a46f8f32d12025-10-08Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 197893
Lithium CarbonateLITHIUM CARBONATEPD-Rx Pharmaceuticals, Inc.c4973d87-d014-42f4-ba13-ae628ca1a4512025-10-08Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 197889
Lithium CarbonateLITHIUM CARBONATEBoswell Pharmacy Services LLC d/b/a BPS Wholesale203386e3-718f-7c84-e063-6394a90aed342024-08-21Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311355
Lithium CarbonateLITHIUM CARBONATENCS HealthCare of KY, LLC dba Vangard Labs204d94de-83e4-400e-bd6b-70b49813802c2023-08-22Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 197889
lithium carbonateLITHIUM CARBONATEBryant Ranch Prepackbfececc8-b2ab-47d1-b126-1c6592bc9c262023-03-28Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 197889
Lithium CarbonateLITHIUM CARBONATEAlembic Pharmaceuticals Limitedd1800f34-3d67-4b2f-874e-8639b125d8532023-01-27Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311355
rxcui: 197893
rxcui: 197889
lithium carbonateLITHIUM CARBONATECamber Pharmaceuticals, Inc.04518b80-7563-4544-bf05-04f286223faa2022-12-26Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311355
rxcui: 197893
rxcui: 197889

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.