lithium

Generic: lithium

Labeler: advagen pharma ltd
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lithium
Generic Name lithium
Labeler advagen pharma ltd
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

lithium citrate 8 meq/5mL

Manufacturer
Advagen Pharma Ltd

Identifiers & Regulatory

Product NDC 72888-172
Product ID 72888-172_47c8d276-05d5-8641-e063-6294a90a8bbc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218036
Listing Expiration 2027-12-31
Marketing Start 2022-11-09

Pharmacologic Class

Classes
mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72888172
Hyphenated Format 72888-172

Supplemental Identifiers

RxCUI
756059
UPC
0372888172460
UNII
5Z6E9K79YV

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 (source: ndc)
Generic Name lithium (source: ndc)
Application Number ANDA218036 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 8 meq/5mL
source: ndc
Packaging
  • 500 mL in 1 BOTTLE (72888-172-46)
source: ndc

Packages (1)

Ingredients (1)

lithium citrate (8 meq/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47c8d276-05d5-8641-e063-6294a90a8bbc", "openfda": {"upc": ["0372888172460"], "unii": ["5Z6E9K79YV"], "rxcui": ["756059"], "spl_set_id": ["ff9baf45-830f-4a8a-8986-5caeaa1b38cf"], "manufacturer_name": ["Advagen Pharma Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BOTTLE (72888-172-46)", "package_ndc": "72888-172-46", "marketing_start_date": "20221109"}], "brand_name": "Lithium", "product_id": "72888-172_47c8d276-05d5-8641-e063-6294a90a8bbc", "dosage_form": "SOLUTION", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "72888-172", "generic_name": "Lithium", "labeler_name": "Advagen Pharma Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium", "active_ingredients": [{"name": "LITHIUM CITRATE", "strength": "8 meq/5mL"}], "application_number": "ANDA218036", "marketing_category": "ANDA", "marketing_start_date": "20221109", "listing_expiration_date": "20271231"}