Lidocaine Hydrochloride and Dextrose
- Product NDC
- 0338-9590
- 11-digit product format
- 003389590
- Labeler code
- 0338
- Product ID
- 0338-9590_fbc0ad14-a653-46b1-9edf-c9682e5cdd9b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine Hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Baxter Healthcare Corpora
- Marketing category
- UNAPPROVED DRUG
- Marketing start
- 2017-10-13
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE HYDRO
- Active strength
- 4 mg/mL
- Pharmacologic classes
- Amide Local Ane
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record