Lidocaine
- Product NDC
- 70518-0854
- 11-digit product format
- 705180854
- Labeler code
- 70518
- Product ID
- 70518-0854_67f3099f-ac05-3b2b-e053-2a91aa0abe00
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040911
- Marketing category
- ANDA
- Marketing start
- 2018-03-21
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE
- Active strength
- 5 g/100g
- Pharmacologic classes
- Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#