lithium

Generic: lithium citrate

Labeler: precision dose, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lithium
Generic Name lithium citrate
Labeler precision dose, inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

lithium citrate 8 meq/5mL

Manufacturer
Precision Dose, Inc.

Identifiers & Regulatory

Product NDC 68094-077
Product ID 68094-077_78d523ef-d924-4154-9b2b-3d5a79a75052
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218036
Listing Expiration 2026-12-31
Marketing Start 2025-10-24

Pharmacologic Class

Classes
mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68094077
Hyphenated Format 68094-077

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 citrate (source: ndc)
Application Number ANDA218036 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 8 meq/5mL
source: ndc
Packaging
  • 3 TRAY in 1 CASE (68094-077-62) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (68094-077-59)
source: ndc

Packages (1)

68094-077-62 3 TRAY in 1 CASE (68094-077-62) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (68094-077-59)

Ingredients (1)

lithium citrate (8 meq/5mL)

Linked Drug Pages (1)

Lithium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "78d523ef-d924-4154-9b2b-3d5a79a75052", "openfda": {"unii": ["5Z6E9K79YV"], "rxcui": ["756059"], "spl_set_id": ["a12d50fb-2c2f-4105-ad17-adbf90d439d4"], "manufacturer_name": ["Precision Dose, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "3 TRAY in 1 CASE (68094-077-62)  / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (68094-077-59)", "package_ndc": "68094-077-62", "marketing_start_date": "20251024"}], "brand_name": "Lithium", "product_id": "68094-077_78d523ef-d924-4154-9b2b-3d5a79a75052", "dosage_form": "SOLUTION", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "68094-077", "generic_name": "Lithium Citrate", "labeler_name": "Precision Dose, 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": "20251024", "listing_expiration_date": "20261231"}