Lidocaine
- Product NDC
- 53217-223
- 11-digit product format
- 532170223
- Labeler code
- 53217
- Product ID
- 53217-223_862bed88-3e87-4d0b-9775-96ea41eed03d
- 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 |
|---|
| 53217-223-30 | Lidocaine | 1 in 1 CARTON | JELLY | 1 | | 2 |
| 53217-223-30 | Lidocaine | 30 mL in 1 TUBE, WITH APPLICATOR | JELLY | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53217-223 | LIDOCAINE (LIDOCAINE HYDROCHLORIDE) JELLY [AIDAREX PHARMACEUTICALS LLC] | 2 | Legacy NDC, 2 package rows | 20161123_46247b76-1ceb-4591-9aad-f5fbb5d5b0b8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53217-223-30 | 53217022330 | 1 in 1 CARTON | Historical |