Lidocaine
- Product NDC
- 71329-401
- 11-digit product format
- 713290401
- Labeler code
- 71329
- Product ID
- 71329-401_bb7bbb1c-b6fc-7026-e053-2a95a90a10fc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- GeneYork Pharmaceuticals Group LLC
- Application
- ANDA212486
- Marketing category
- ANDA
- Marketing start
- 2021-02-16
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE
- Active strength
- 50 mg/g
- Pharmacologic classes
- Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71329-401-06 | 71329040106 | 1 TUBE in 1 CARTON (71329-401-06) > 35.44 g in 1 TUBE | 1 tube | 2021-02-16 | 0000-00-00 | No | No | Current |