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NDC 71205-0356-20 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 Proficient Rx LP. The primary component is CYCLOBENZAPRINE HYDROCHLORIDE.
Product Information
NDC | 71205-0356 |
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Product ID | 71205-356_b8f42c39-b984-478f-a2b8-97209a356960 |
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 | Proficient Rx LP |
Pharmaceutical Class | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA208170 |
Listing Certified Through | 2025-12-31 |
Package
NDC 71205-0356-20 (71205035620)
NDC Package Code | 71205-356-20 |
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Billing NDC | 71205035620 |
Package | 20 TABLET, FILM COATED in 1 BOTTLE (71205-356-20) |
Marketing Start Date | 2023-04-06 |
NDC Exclude Flag | N |
Pricing Information | N/A |