NDC 68094-757

Lithium

Lithium

Lithium is a Oral Solution in the Human Prescription Drug category. It is labeled and distributed by Precision Dose Inc.. The primary component is Lithium Citrate.

• Product ID: 68094-757_6ad1ae07-1d53-486b-a7a2-daba3f772164
• NDC: 68094-757
• Product Type: Human Prescription Drug
• Proprietary Name: Lithium
• Generic Name: Lithium
• Dosage Form: Solution
• Route of Administration: ORAL
• Marketing Start Date: 2012-10-25
• Marketing Category: NDA / NDA
• Application Number: NDA018421
• Labeler Name: Precision Dose Inc.
• Substance Name: LITHIUM CITRATE
• Active Ingredient Strength: 8 meq/5mL
• Pharm Classes: Mood Stabilizer [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 68094-757-62

3 TRAY in 1 CASE (68094-757-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (68094-757-59)

• Marketing Start Date: 2012-10-25
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68094-757-59 [68094075759]

Lithium SOLUTION

• Marketing Category: NDA
• Application Number: NDA018421
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2012-10-25

NDC 68094-757-62 [68094075762]

Lithium SOLUTION

• Marketing Category: NDA
• Application Number: NDA018421
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2012-10-25

Drug Details

Active Ingredients

Ingredient	Strength
LITHIUM CITRATE	8 meq/5mL

OpenFDA Data

• SPL SET ID: 1a04cc23-61fa-455b-9718-2cdcf54036e0
• Manufacturer:
  • Precision Dose Inc.
• UNII:
  • 5Z6E9K79YV
• RxNorm Concept Unique ID - RxCUI:
  • 756059

Pharmacological Class

• Mood Stabilizer [EPC]

NDC Crossover Matching brand name "Lithium" or generic name "Lithium"

NDC	Brand Name	Generic Name
0054-3527	Lithium	Lithium
60986-1019	Lithium	Lithium Bromatum
68094-757	Lithium	Lithium