LIDOCAINE
- Product NDC
- 76074-135
- 11-digit product format
- 760740135
- Labeler code
- 76074
- Product ID
- 76074-135_6fa06fbd-1f94-4829-bc7d-9b4aebefa917
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LIDOCAINE
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Two Hip Consulting, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2016-03-25
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE
- Active strength
- 5 g/100g
- Pharmacologic classes
- Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76074-135-11 | LIDOCAINE | 50 g in 1 TUBE | OINTMENT | 50 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76074-135 | LIDOCAINE OINTMENT [TWO HIP CONSULTING, LLC] | 3 | Legacy NDC, 1 package rows | 20190207_d5e2e8c0-48b3-4666-95a2-d9aef29f1a1c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 76074-135-11 | 76074013511 | 50 g in 1 TUBE | 50 g | Historical |