LIDOCAINE
- Product NDC
- 52959-993
- 11-digit product format
- 529590993
- Labeler code
- 52959
- Product ID
- 52959-993_77bdaf2b-4506-115e-e053-2991aa0ad5ec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LIDOCAINE
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- H.J. Harkins Company, Inc.
- Application
- ANDA207810
- Marketing category
- ANDA
- Marketing start
- 2018-10-08
- 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
- 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 |
|---|
| 52959-993-50 | LIDOCAINE | 50 g in 1 TUBE | OINTMENT | 50 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52959-993 | LIDOCAINE OINTMENT [H.J. HARKINS COMPANY, INC.] | 1 | Legacy NDC, 1 package rows | 20181010_77bdaf2b-4505-115e-e053-2991aa0ad5ec.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 52959-993-50 | 52959099350 | 50 g in 1 TUBE | 50 g | Historical |