lithium

Generic: lithium

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lithium
Generic Name lithium
Labeler remedyrepack inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

lithium citrate 8 meq/5mL

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4227
Product ID 70518-4227_400519aa-488a-40e4-e063-6394a90a8d39
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218036
Listing Expiration 2026-12-31
Marketing Start 2024-11-04

Pharmacologic Class

Classes
mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184227
Hyphenated Format 70518-4227

Supplemental Identifiers

RxCUI
756059
UNII
5Z6E9K79YV

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
  • 10 CUP in 1 BOX (70518-4227-0) / 5 mL in 1 CUP (70518-4227-1)
  • 10 CUP, UNIT-DOSE in 1 BOX (70518-4227-2) / 10 mL in 1 CUP, UNIT-DOSE (70518-4227-3)
source: ndc

Packages (2)

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": "400519aa-488a-40e4-e063-6394a90a8d39", "openfda": {"unii": ["5Z6E9K79YV"], "rxcui": ["756059"], "spl_set_id": ["be1346df-4a39-45e8-874b-e2a496847fd5"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "10 CUP in 1 BOX (70518-4227-0)  / 5 mL in 1 CUP (70518-4227-1)", "package_ndc": "70518-4227-0", "marketing_start_date": "20241104"}, {"sample": false, "description": "10 CUP, UNIT-DOSE in 1 BOX (70518-4227-2)  / 10 mL in 1 CUP, UNIT-DOSE (70518-4227-3)", "package_ndc": "70518-4227-2", "marketing_start_date": "20241105"}], "brand_name": "Lithium", "product_id": "70518-4227_400519aa-488a-40e4-e063-6394a90a8d39", "dosage_form": "SOLUTION", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "70518-4227", "generic_name": "Lithium", "labeler_name": "REMEDYREPACK INC.", "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": "20241104", "listing_expiration_date": "20261231"}