lithium carbonate er

Generic: lithium carbonate

Labeler: glenmark pharmaceuticals inc., usa
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lithium carbonate er
Generic Name lithium carbonate
Labeler glenmark pharmaceuticals inc., usa
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lithium carbonate 450 mg/1

Manufacturer
Glenmark Pharmaceuticals Inc., USA

Identifiers & Regulatory

Product NDC 68462-224
Product ID 68462-224_0072bf62-84d4-426b-aa03-bb7f8fef21c9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091616
Listing Expiration 2027-12-31
Marketing Start 2011-02-14

Pharmacologic Class

Classes
mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68462224
Hyphenated Format 68462-224

Supplemental Identifiers

RxCUI
197892
UPC
0368462224014
UNII
2BMD2GNA4V

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name lithium carbonate er (source: ndc)
Generic Name lithium carbonate (source: ndc)
Application Number ANDA091616 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 450 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68462-224-01)
  • 1000 TABLET in 1 BOTTLE (68462-224-10)
  • 30 TABLET in 1 BOTTLE (68462-224-30)
source: ndc

Packages (3)

68462-224-01 100 TABLET in 1 BOTTLE (68462-224-01) 68462-224-10 1000 TABLET in 1 BOTTLE (68462-224-10) 68462-224-30 30 TABLET in 1 BOTTLE (68462-224-30)

Ingredients (1)

lithium carbonate (450 mg/1)

Linked Drug Pages (1)

Lithium Carbonate ER ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0072bf62-84d4-426b-aa03-bb7f8fef21c9", "openfda": {"upc": ["0368462224014"], "unii": ["2BMD2GNA4V"], "rxcui": ["197892"], "spl_set_id": ["525a9d9b-cbb1-4644-a28a-8bba96f09348"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68462-224-01)", "package_ndc": "68462-224-01", "marketing_start_date": "20110214"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (68462-224-10)", "package_ndc": "68462-224-10", "marketing_start_date": "20110214"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68462-224-30)", "package_ndc": "68462-224-30", "marketing_start_date": "20110214"}], "brand_name": "Lithium Carbonate ER", "product_id": "68462-224_0072bf62-84d4-426b-aa03-bb7f8fef21c9", "dosage_form": "TABLET", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "68462-224", "generic_name": "Lithium Carbonate", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium Carbonate", "brand_name_suffix": "ER", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "450 mg/1"}], "application_number": "ANDA091616", "marketing_category": "ANDA", "marketing_start_date": "20110214", "listing_expiration_date": "20271231"}