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NDC 68788-7018-06 Metaxalone 800 mg/1 Details
Metaxalone 800 mg/1
Metaxalone is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is METAXALONE.
MedlinePlus Drug Summary
Metaxalone, a muscle relaxant, is used with rest, physical therapy, and other measures to relax muscles and relieve pain and discomfort caused by strains, sprains, and other muscle injuries.
Related Packages: 68788-7018-06Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Metaxalone
Product Information
| NDC | 68788-7018 |
|---|---|
| Product ID | 68788-7018_70fc9abd-d193-4364-8172-ad77e46deb3a |
| Associated GPIs | 75100060000320 |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Metaxalone |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Metaxalone |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 800 |
| Active Ingredient Units | mg/1 |
| Substance Name | METAXALONE |
| Labeler Name | Preferred Pharmaceuticals Inc. |
| Pharmaceutical Class | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA203695 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 68788-7018-06 (68788701806)
| NDC Package Code | 68788-7018-6 |
|---|---|
| Billing NDC | 68788701806 |
| Package | 60 TABLET in 1 BOTTLE (68788-7018-6) |
| Marketing Start Date | 2017-10-11 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |