Mexiletine Hydrochloride
- Product NDC
- 72162-1774
- 11-digit product format
- 721621774
- Labeler code
- 72162
- Product ID
- 72162-1774_c6c4c877-bdcb-464b-813c-39ebfb279253
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mexiletine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074450
- Marketing category
- ANDA
- Marketing start
- 2020-06-22
- Substance
- MEXILETINE HYDROCHLORIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Mexiletine Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MEXILETINE HYDROCHLORIDE | 250 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 606D60IS38 |
| Rxcui | 1362720 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1774-1 | Mexiletine Hydrochloride | 100 in 1 BOTTLE | CAPSULE | 100 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1774 | MEXILETINE HYDROCHLORIDE CAPSULE [BRYANT RANCH PREPACK] | 100 | Current NDC, 1 package rows | 20240208_e2c0430d-35ee-460c-b0d5-f117d43430c5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1774-1 | 72162177401 | 100 CAPSULE in 1 BOTTLE (72162-1774-1) | 100 capsule | 2026-03-25 | No | No | Historical |