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NDC 50090-1848-01 Cyclobenzaprine Hydrochloride 7.5 mg/1 Details
Cyclobenzaprine Hydrochloride 7.5 mg/1
Cyclobenzaprine Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is CYCLOBENZAPRINE HYDROCHLORIDE.
Product Information
NDC | 50090-1848 |
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Product ID | 50090-1848_e50a2157-5f9c-4c84-9f26-61383e406c9a |
Associated GPIs | 75100050100304 |
GCN Sequence Number | 062524 |
GCN Sequence Number Description | cyclobenzaprine HCl TABLET 7.5 MG ORAL |
HIC3 | H6H |
HIC3 Description | SKELETAL MUSCLE RELAXANTS |
GCN | 98299 |
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 | 7.5 |
Active Ingredient Units | mg/1 |
Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
Labeler Name | A-S Medication Solutions |
Pharmaceutical Class | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA078722 |
Listing Certified Through | 2024-12-31 |
Package
NDC 50090-1848-01 (50090184801)
NDC Package Code | 50090-1848-1 |
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Billing NDC | 50090184801 |
Package | 30 TABLET, FILM COATED in 1 BOTTLE (50090-1848-1) |
Marketing Start Date | 2015-05-28 |
NDC Exclude Flag | N |
Pricing Information | N/A |