lithium
Generic: lithium
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
lithium
Generic Name
lithium
Labeler
remedyrepack inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
lithium citrate 8 meq/5mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184227
Hyphenated Format
70518-4227
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 8 meq/5mL
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)
Packages (2)
Ingredients (1)
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"}