ALLERGY 24-HR is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Wockhardt Usa Llc.. The primary component is Fexofenadine Hydrochloride.
Product ID | 64679-987_6633dc75-e76d-48f1-a47f-3cc454d7c042 |
NDC | 64679-987 |
Product Type | Human Otc Drug |
Proprietary Name | ALLERGY 24-HR |
Generic Name | Fexofenadine Hydrochloride |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 2012-02-08 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA079112 |
Labeler Name | Wockhardt USA LLC. |
Substance Name | FEXOFENADINE HYDROCHLORIDE |
Active Ingredient Strength | 180 mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2012-02-08 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA079112 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-02-08 |
Marketing Category | ANDA |
Application Number | ANDA079112 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-02-08 |
Marketing Category | ANDA |
Application Number | ANDA079112 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-02-08 |
Marketing Category | ANDA |
Application Number | ANDA079112 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-02-08 |
Marketing Category | ANDA |
Application Number | ANDA079112 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-02-08 |
Marketing Category | ANDA |
Application Number | ANDA079112 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-02-08 |
Marketing Category | ANDA |
Application Number | ANDA079112 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-02-08 |
Marketing Category | ANDA |
Application Number | ANDA079112 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-02-08 |
Marketing Category | ANDA |
Application Number | ANDA079112 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-02-08 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA079112 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-02-08 |
Marketing Category | ANDA |
Application Number | ANDA079112 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA079112 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-02-08 |
Marketing Category | ANDA |
Application Number | ANDA079112 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-02-08 |
Marketing Category | ANDA |
Application Number | ANDA079112 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-02-08 |
Ingredient | Strength |
---|---|
FEXOFENADINE HYDROCHLORIDE | 180 mg/1 |
SPL SET ID: | f4b394a6-8b4d-41ac-8962-82e81d85dd90 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
64679-987 | ALLERGY 24-HR | ALLERGY 24-HR |
64679-982 | ALLERGY 24-HR | ALLERGY 24-HR |
64679-744 | ALLERGY 24-HR | ALLERGY 24-HR |
10202-107 | Allergy | Fexofenadine hydrochloride |
11822-0425 | allergy relief | fexofenadine hydrochloride |
11822-0571 | allergy relief | fexofenadine hydrochloride |
11822-3698 | Allergy Relief | Fexofenadine hydrochloride |
21130-784 | Allergy Relief | Fexofenadine hydrochloride |
0363-0095 | Fexofenadine hydrochloride | Fexofenadine hydrochloride |
0363-0097 | Fexofenadine hydrochloride | Fexofenadine hydrochloride |
0363-0783 | Fexofenadine hydrochloride | Fexofenadine hydrochloride |
0363-9898 | Fexofenadine Hydrochloride | Fexofenadine Hydrochloride |
0615-5619 | Fexofenadine Hydrochloride | Fexofenadine Hydrochloride |
0615-5620 | Fexofenadine Hydrochloride | Fexofenadine Hydrochloride |
0615-7636 | Fexofenadine Hydrochloride | Fexofenadine Hydrochloride |
0904-5961 | Fexofenadine Hydrochloride | Fexofenadine Hydrochloride |
0904-5962 | Fexofenadine Hydrochloride | Fexofenadine Hydrochloride |
0904-5963 | Fexofenadine Hydrochloride | Fexofenadine Hydrochloride |
0904-6214 | fexofenadine hydrochloride | fexofenadine hydrochloride |
0904-6711 | Fexofenadine hydrochloride | Fexofenadine hydrochloride |
10202-229 | Fexofenadine hydrochloride | Fexofenadine hydrochloride |
13107-066 | Fexofenadine hydrochloride | Fexofenadine hydrochloride |
13107-067 | Fexofenadine hydrochloride | Fexofenadine hydrochloride |
21695-461 | Fexofenadine Hydrochloride | Fexofenadine Hydrochloride |
21695-462 | Fexofenadine Hydrochloride | Fexofenadine Hydrochloride |
30142-878 | Fexofenadine hydrochloride | Fexofenadine hydrochloride |
0179-8325 | Fexofenadine Hydrochloride 180 | Fexofenadine Hydrochloride |
0113-0571 | good sense aller ease | fexofenadine hydrochloride |
0113-0847 | good sense aller ease | fexofenadine hydrochloride |
11673-571 | up and up allergy relief | fexofenadine hydrochloride |
11673-617 | up and up allergy relief | fexofenadine hydrochloride |
11673-800 | up and up allergy relief | Fexofenadine Hydrochloride |
0363-0571 | wal fex allergy | fexofenadine hydrochloride |
0363-0784 | Wal-Fex | Fexofenadine hydrochloride |