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
Label	Manufacturer	Effective date	Type
Lithium Carbonate - Alembic Limited	Alembic Limited	2009-01-27	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
46708-014-30	Lithium Carbonate	30 in 1 BOTTLE	CAPSULE	30	1
46708-014-31	Lithium Carbonate	100 in 1 BOTTLE	CAPSULE	100	1
46708-014-71	Lithium Carbonate	500 in 1 BOTTLE	CAPSULE	500	1
46708-014-91	Lithium Carbonate	1000 in 1 BOTTLE	CAPSULE	1000	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
46708-014	LITHIUM CARBONATE CAPSULE [ALEMBIC LIMITED]	1	4 package rows	20090212_083ca85f-a450-4fe9-973e-47a13cd18dd1.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
lithium carbonate	ACTIVE INGREDIENT	2BMD2GNA4V	LITHIUM CARBONATE CAPSULE [ALEMBIC LIMITED]	1
lithium cation	ACTIVE MOIETY	8H8Z5UER66	LITHIUM CARBONATE CAPSULE [ALEMBIC LIMITED]	1
black iron oxide	INACTIVE INGREDIENT		LITHIUM CARBONATE CAPSULE [ALEMBIC LIMITED]	1
D&C Yellow No. 10	INACTIVE INGREDIENT		LITHIUM CARBONATE CAPSULE [ALEMBIC LIMITED]	1
FD&C Red No. 40	INACTIVE INGREDIENT		LITHIUM CARBONATE CAPSULE [ALEMBIC LIMITED]	1
FD&C Yellow No. 6	INACTIVE INGREDIENT		LITHIUM CARBONATE CAPSULE [ALEMBIC LIMITED]	1
gelatin	INACTIVE INGREDIENT	2G86QN327L	LITHIUM CARBONATE CAPSULE [ALEMBIC LIMITED]	1
talc	INACTIVE INGREDIENT	7SEV7J4R1U	LITHIUM CARBONATE CAPSULE [ALEMBIC LIMITED]	1
titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	LITHIUM 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 2 of 2 · 25 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Lithium Carbonate	LITHIUM CARBONATE	Hikma Pharmaceuticals USA Inc.	7dc9c6d2-6d9a-49e4-a8ab-437b0ed5f84e	2022-11-22	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 311355 rxcui: 197893 rxcui: 197889
LITHIUM CARBONATE LITHIUM CARBONATE	LITHIUM CARBONATE	Alembic Pharmaceuticals Inc.	4ca2b977-b94c-4232-9b7e-835db97c9544	2022-11-03	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 311355 rxcui: 197893 rxcui: 197889
lithium carbonate	LITHIUM CARBONATE	Aphena Pharma Solutions - Tennessee, LLC	2b81eabc-5c5a-4b63-88d4-3f13b45a683e	2021-06-24	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 197889
Lithium Carbonate	LITHIUM CARBONATE	Proficient Rx LP	d3291474-8ef2-4cd8-aecc-2f550fd6a299	2021-01-01	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 197889
8B9E83E5-EB7D-791A-AD07-492D86E89EC7			083ca85f-a450-4fe9-973e-47a13cd18dd1	2009-01-27	Boxed warning, Warnings, Adverse reactions	Exact identifier spl id: 8B9E83E5-EB7D-791A-AD07-492D86E89EC7 spl set id: 083ca85f-a450-4fe9-973e-47a13cd18dd1

Reported adverse events (FAERS/openFDA)#

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