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NDC 76420-0033-90 Cyclobenzaprine Hydrochloride 10 mg/1 Details
Cyclobenzaprine Hydrochloride 10 mg/1
Cyclobenzaprine Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Asclemed USA, Inc.. The primary component is CYCLOBENZAPRINE HYDROCHLORIDE.
Product Information
NDC | 76420-0033 |
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Product ID | 76420-033_f5f82b93-a80e-3ab8-e053-2995a90a68f5 |
Associated GPIs | 75100050100305 |
GCN Sequence Number | 004681 |
GCN Sequence Number Description | cyclobenzaprine HCl TABLET 10 MG ORAL |
HIC3 | H6H |
HIC3 Description | SKELETAL MUSCLE RELAXANTS |
GCN | 18020 |
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 | 10 |
Active Ingredient Units | mg/1 |
Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
Labeler Name | Asclemed USA, Inc. |
Pharmaceutical Class | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA077797 |
Listing Certified Through | 2024-12-31 |
Package
NDC 76420-0033-90 (76420003390)
NDC Package Code | 76420-033-90 |
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Billing NDC | 76420003390 |
Package | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-033-90) |
Marketing Start Date | 2023-03-03 |
NDC Exclude Flag | N |
Pricing Information | N/A |