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NDC 72789-0122-30 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 PD-Rx 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: 72789-0122-30Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Metaxalone
Product Information
| NDC | 72789-0122 |
|---|---|
| Product ID | 72789-122_0632aa0a-3d3a-374f-e063-6394a90a52c4 |
| Associated GPIs | 75100060000320 |
| GCN Sequence Number | 051112 |
| GCN Sequence Number Description | metaxalone TABLET 800 MG ORAL |
| HIC3 | H6H |
| HIC3 Description | SKELETAL MUSCLE RELAXANTS |
| GCN | 91765 |
| HICL Sequence Number | 001945 |
| HICL Sequence Number Description | METAXALONE |
| Brand/Generic | Generic |
| 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 | PD-Rx Pharmaceuticals, Inc. |
| Pharmaceutical Class | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA208774 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 72789-0122-30 (72789012230)
| NDC Package Code | 72789-122-30 |
|---|---|
| Billing NDC | 72789012230 |
| Package | 90 TABLET in 1 BOTTLE, PLASTIC (72789-122-30) |
| Marketing Start Date | 2020-09-25 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |