NDC 0363-0784
Wal-Fex
Fexofenadine Hydrochloride
Wal-Fex 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 ID | 0363-0784_02b6f599-0ce7-6ade-d1a9-6aa7310d12c2 |
| NDC | 0363-0784 |
| Product Type | Human Otc Drug |
| Proprietary Name | Wal-Fex |
| Generic Name | Fexofenadine Hydrochloride |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2011-04-13 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA076502 |
| Labeler Name | Walgreens Company |
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
| Active Ingredient Strength | 180 mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
Packaging
NDC 0363-0784-07
1 BLISTER PACK in 1 CARTON (0363-0784-07) > 5 TABLET in 1 BLISTER PACK
| Marketing Start Date | 2011-04-13 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 0363-0784-07 [00363078407]
Wal-Fex TABLET
| Marketing Category | ANDA |
| Application Number | ANDA076502 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-04-13 |
NDC 0363-0784-90 [00363078490]
Wal-Fex TABLET
| Marketing Category | ANDA |
| Application Number | ANDA076502 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-04-13 |
NDC 0363-0784-40 [00363078440]
Wal-Fex TABLET
| Marketing Category | ANDA |
| Application Number | ANDA076502 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-04-13 |
NDC 0363-0784-30 [00363078430]
Wal-Fex TABLET
| Marketing Category | ANDA |
| Application Number | ANDA076502 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-04-13 |
NDC 0363-0784-75 [00363078475]
Wal-Fex TABLET
| Marketing Category | ANDA |
| Application Number | ANDA076502 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-04-13 |
NDC 0363-0784-43 [00363078443]
Wal-Fex TABLET
| Marketing Category | ANDA |
| Application Number | ANDA076502 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-04-13 |
NDC 0363-0784-29 [00363078429]
Wal-Fex TABLET
| Marketing Category | ANDA |
| Application Number | ANDA076502 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-04-13 |
NDC 0363-0784-15 [00363078415]
Wal-Fex TABLET
| Marketing Category | ANDA |
| Application Number | ANDA076502 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-04-13 |
NDC 0363-0784-45 [00363078445]
Wal-Fex TABLET
| Marketing Category | ANDA |
| Application Number | ANDA076502 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-04-13 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| FEXOFENADINE HYDROCHLORIDE | 180 mg/1 |
OpenFDA Data
| SPL SET ID: | 95d420ea-6337-304f-54c3-0c75be1608e2 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
NDC Crossover Matching brand name "Wal-Fex" or generic name "Fexofenadine Hydrochloride"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0363-0784 | Wal-Fex | Fexofenadine hydrochloride |
| 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 |
Trademark Results [Wal-Fex]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 WAL-FEX 85228565 4085088 Live/Registered |
Walgreen Co. 2011-01-28 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.