Quinidine Gluconate
- Product NDC
- 0002-1407
- 11-digit product format
- 000021407
- Labeler code
- 0002
- Product ID
- 0002-1407_14757f9d-f641-4836-acf3-229265588d1d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quinidine Gluconate
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Eli Lilly and Company
- Application
- NDA007529
- Marketing category
- NDA
- Marketing start
- 1950-07-12
- Marketing end
- 0000-00-00
- Substance
- QUINIDINE GLUCONATE
- Active strength
- 80 mg/mL
- Pharmacologic classes
- Antiarrhythmic [EPC],Cytochrome P450 2D6 Inhibitor [EPC],Cytochrome P450 2D6 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record