Mexiletine Hydrochloride
- Product NDC
- 68151-2986
- 11-digit product format
- 681512986
- Labeler code
- 68151
- Product ID
- 68151-2986_3a464dbd-3b36-467f-a22a-ba9617189459
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mexiletine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA074377
- Marketing category
- ANDA
- Marketing start
- 1995-06-05
- Marketing end
- 0000-00-00
- Substance
- MEXILETINE HYDROCHLORIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 68151-2986-0 | Mexiletine Hydrochloride | 1 in 1 PACKAGE | CAPSULE | 1 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-2986 | MEXILETINE HYDROCHLORIDE CAPSULE [CARILION MATERIALS MANAGEMENT] | 3 | Legacy NDC, 1 package rows | 20160805_bb8c0b61-fcb1-4b51-9505-f1670693f00f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-2986-0 | 68151298600 | 1 in 1 PACKAGE | Historical |