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NDC 72189-0280-15 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 DirectRx. The primary component is CYCLOBENZAPRINE HYDROCHLORIDE.
Product Information
NDC | 72189-0280 |
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Product ID | 72189-280_0c41e3a6-4386-e05b-e063-6394a90a5dad |
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 | DirectRx |
Pharmaceutical Class | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA213324 |
Listing Certified Through | 2024-12-31 |
Package
NDC 72189-0280-15 (72189028015)
NDC Package Code | 72189-280-15 |
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Billing NDC | 72189028015 |
Package | 15 TABLET, FILM COATED in 1 BOTTLE (72189-280-15) |
Marketing Start Date | 2021-10-07 |
NDC Exclude Flag | N |
Pricing Information | N/A |