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NDC 70934-0667-30 Cyclobenzaprine Hydrochloride 5 mg/1 Details
Cyclobenzaprine Hydrochloride 5 mg/1
Cyclobenzaprine Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. dba Northwind Pharmaceuticals. The primary component is CYCLOBENZAPRINE HYDROCHLORIDE.
MedlinePlus Drug Summary
Cyclobenzaprine 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. Cyclobenzaprine is in a class of medications called skeletal muscle relaxants. It works by acting in the brain and nervous system to allow the muscles to relax.
Related Packages: 70934-0667-30Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Cyclobenzaprine
Product Information
| NDC | 70934-0667 |
|---|---|
| Product ID | 70934-667_be5e7c66-1493-20d0-e053-2a95a90a681b |
| Associated GPIs | 75100050100303 |
| GCN Sequence Number | 047478 |
| GCN Sequence Number Description | cyclobenzaprine HCl TABLET 5 MG ORAL |
| HIC3 | H6H |
| HIC3 Description | SKELETAL MUSCLE RELAXANTS |
| GCN | 12805 |
| HICL Sequence Number | 001950 |
| HICL Sequence Number Description | CYCLOBENZAPRINE HCL |
| Brand/Generic | Generic |
| Proprietary Name | Cyclobenzaprine Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Cyclobenzaprine Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 5 |
| Active Ingredient Units | mg/1 |
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
| Labeler Name | Denton Pharma, Inc. dba Northwind Pharmaceuticals |
| Pharmaceutical Class | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA078048 |
| Listing Certified Through | 2022-12-31 |
Package
NDC 70934-0667-30 (70934066730)
| NDC Package Code | 70934-667-30 |
|---|---|
| Billing NDC | 70934066730 |
| Package | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-667-30) |
| Marketing Start Date | 2020-04-14 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |