Isolyte S in Dextrose
- Product NDC
- 0264-7704
- 11-digit product format
- 002647704
- Labeler code
- 0264
- Product ID
- 0264-7704_cb81fe4a-10a7-4e24-aa4f-b4315fcfe39b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrous Dextrose, Sodium Chloride, Sodium Gluconate, Sodium Acetate Trihydrate, Potassium Chloride a
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- B. Braun Medical Inc.
- Application
- ANDA019843
- Marketing category
- ANDA
- Marketing start
- 1993-08-09
- Marketing end
- 0000-00-00
- Substance
- DEXTROSE; SODIU
- Active strength
- 5 g/100mL; g/100m
- Pharmacologic classes
- Osmotic Laxativ
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record