Lidocaine and Prilocaine
- Product NDC
- 63739-054
- 11-digit product format
- 637390054
- Labeler code
- 63739
- Product ID
- 63739-054_9b924815-f957-45d0-b4b4-44a8c41aa7b8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine and Prilocaine
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- McKesson Corporation
- Application
- ANDA205887
- Marketing category
- ANDA
- Marketing start
- 2018-06-29
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE; PRILOCAINE
- Active strength
- 25 mg/g; mg/g
- Pharmacologic classes
- Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE],Amide Local Anesthetic [EPC],Amides [CS],Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-054-66 | 63739005466 | 1 TUBE in 1 CARTON (63739-054-66) > 30 g in 1 TUBE | 1 tube | 2021-05-24 | 0000-00-00 | No | No | Current |