Eha
- Product NDC
- 76420-351
- 11-digit product format
- 764200351
- Labeler code
- 76420
- Product ID
- 76420-351_7d77ecf6-5731-d43e-e053-2991aa0af0db
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine Hydrochloride
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Asclemed USA, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2016-06-07
- Substance
- LIDOCAINE HYDROCHLORIDE
- Active strength
- 4 g/mL
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Eha
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LIDOCAINE HYDROCHLORIDE | 4 g/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V13007Z41A |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76420-351-30 | Eha | 88 mL in 1 BOTTLE | LOTION | 88 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76420-351 | EHA (LIDOCAINE HYDROCHLORIDE) LOTION [ASCLEMED USA, INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20181221_09835640-55c3-4bfa-9ad3-15d37f06e871.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76420-351-30 | 76420035130 | 88 mL in 1 BOTTLE (76420-351-30) | 88 ml | 2016-06-07 | 0000-00-00 | No | No | Current |