Lidocaine
- Product NDC
- 53217-222
- 11-digit product format
- 532170222
- Labeler code
- 53217
- Product ID
- 53217-222_bd9f145d-155d-4482-86b0-882856ce435f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine Hydrochloride
- Dosage form
- JELLY
- Route
- TOPICAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA040837
- Marketing category
- ANDA
- Marketing start
- 2015-06-15
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE HYDROCHLORIDE
- Active strength
- 20 mg/mL
- 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53217-222-01 | Lidocaine | 1 in 1 CARTON | JELLY | 1 | | 2 |
| 53217-222-01 | Lidocaine | 5 mL in 1 TUBE, WITH APPLICATOR | JELLY | 5 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53217-222 | LIDOCAINE (LIDOCAINE HYDROCHLORIDE) JELLY [AIDAREX PHARMACEUTICALS LLC] | 2 | Legacy NDC, 2 package rows | 20161122_008e8da2-1390-457b-89dd-41de33611942.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53217-222-01 | 53217022201 | 1 in 1 CARTON | Historical |