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NDC 72835-0601-02 Quinixil Details
Quinixil
Quinixil is a KIT in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by V2 Pharma, LLC. The primary component is .
Product Information
NDC | 72835-0601 |
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Product ID | 72835-601_6508f6db-0e5e-46c7-a596-4bb5222a4d3d |
Associated GPIs | 9055990290B120 |
GCN Sequence Number | 080080 |
GCN Sequence Number Description | mometasone furoate/dimethicone CREAM (G) 0.1 %-5 % TOPICAL |
HIC3 | Q5P |
HIC3 Description | TOPICAL ANTI-INFLAMMATORY STEROIDAL |
GCN | 46767 |
HICL Sequence Number | 045918 |
HICL Sequence Number Description | MOMETASONE FUROATE/DIMETHICONE |
Brand/Generic | Brand |
Proprietary Name | Quinixil |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Mometasone Furoate and Dimethicone |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | KIT |
Route | n/a |
Active Ingredient Strength | n/a |
Active Ingredient Units | n/a |
Substance Name | n/a |
Labeler Name | V2 Pharma, LLC |
Pharmaceutical Class | n/a |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA076216 |
Listing Certified Through | 2024-12-31 |
Package
NDC 72835-0601-02 (72835060102)
NDC Package Code | 72835-601-02 |
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Billing NDC | 72835060102 |
Package | 1 KIT in 1 CARTON (72835-601-02) * 1 TUBE in 1 CARTON (0713-0634-37) / 45 g in 1 TUBE * 114 g in 1 TUBE (69740-322-00) |
Marketing Start Date | 2019-06-03 |
NDC Exclude Flag | N |
Pricing Information | N/A |