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NDC 00363-0783-24 Fexofenadine hydrochloride 60 mg/1 Details
Fexofenadine hydrochloride 60 mg/1
Fexofenadine hydrochloride is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Walgreens Company. The primary component is FEXOFENADINE HYDROCHLORIDE.
Product Information
NDC | 00363-0783 |
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Product ID | 0363-0783_90bff7b8-9a61-b05c-2408-c08b1eb50c66 |
Associated GPIs | |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | Fexofenadine hydrochloride |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Fexofenadine hydrochloride |
Product Type | HUMAN OTC DRUG |
Dosage Form | TABLET |
Route | ORAL |
Active Ingredient Strength | 60 |
Active Ingredient Units | mg/1 |
Substance Name | FEXOFENADINE HYDROCHLORIDE |
Labeler Name | Walgreens Company |
Pharmaceutical Class | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA076502 |
Listing Certified Through | 2024-12-31 |
Package
NDC 00363-0783-24 (00363078324)
NDC Package Code | 0363-0783-24 |
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Billing NDC | 00363078324 |
Package | 4 BLISTER PACK in 1 CARTON (0363-0783-24) / 6 TABLET in 1 BLISTER PACK |
Marketing Start Date | 2020-12-14 |
NDC Exclude Flag | N |
Pricing Information | N/A |