Mexiletine Hydrochloride
- Product NDC
- 63629-1962
- 11-digit product format
- 636291962
- Labeler code
- 63629
- Product ID
- 63629-1962_8c03628f-61a2-4b17-a615-b1d57d1975c3
- 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
- Marketing end
- 0000-00-00
- Substance
- MEXILETINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-1962-1 | 63629196201 | 100 CAPSULE in 1 BOTTLE (63629-1962-1) | 100 capsule | 2021-01-14 | 0000-00-00 | No | No | Current |