NDC 0363-0010
Wal-Zan
Ranitidine Hydrochloride Tablets 150mg
Wal-Zan is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Walgreens Company. The primary component is Ranitidine Hydrochloride.
| Product ID | 0363-0010_9b415007-a9fb-03b9-b8ec-5f96d120f040 |
| NDC | 0363-0010 |
| Product Type | Human Otc Drug |
| Proprietary Name | Wal-Zan |
| Generic Name | Ranitidine Hydrochloride Tablets 150mg |
| Dosage Form | Tablet, Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2011-06-11 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA078192 |
| Labeler Name | Walgreens Company |
| Substance Name | RANITIDINE HYDROCHLORIDE |
| Active Ingredient Strength | 150 mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
Packaging
NDC 0363-0010-01
1 BOTTLE in 1 CARTON (0363-0010-01) > 200 TABLET, COATED in 1 BOTTLE
| Marketing Start Date | 2011-06-11 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 0363-0010-61 [00363001061]
Wal-Zan TABLET, COATED
| Marketing Category | ANDA |
| Application Number | ANDA078192 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-06-11 |
NDC 0363-0010-23 [00363001023]
Wal-Zan TABLET, COATED
| Marketing Category | ANDA |
| Application Number | ANDA078192 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-06-11 |
NDC 0363-0010-01 [00363001001]
Wal-Zan TABLET, COATED
| Marketing Category | ANDA |
| Application Number | ANDA078192 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-06-11 |
NDC 0363-0010-32 [00363001032]
Wal-Zan TABLET, COATED
| Marketing Category | ANDA |
| Application Number | ANDA078192 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-06-11 |
NDC 0363-0010-26 [00363001026]
Wal-Zan TABLET, COATED
| Marketing Category | ANDA |
| Application Number | ANDA078192 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-06-11 |
NDC 0363-0010-62 [00363001062]
Wal-Zan TABLET, COATED
| Marketing Category | ANDA |
| Application Number | ANDA078192 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-06-11 |
NDC 0363-0010-34 [00363001034]
Wal-Zan TABLET, COATED
| Marketing Category | ANDA |
| Application Number | ANDA078192 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-06-11 |
NDC 0363-0010-50 [00363001050]
Wal-Zan TABLET, COATED
| Marketing Category | ANDA |
| Application Number | ANDA078192 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-06-11 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| RANITIDINE HYDROCHLORIDE | 150 mg/1 |
OpenFDA Data
| SPL SET ID: | 9f7d916b-1624-5cf6-2394-50a557c016ad |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
NDC Crossover Matching brand name "Wal-Zan" or generic name "Ranitidine Hydrochloride Tablets 150mg"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0363-0010 | Wal-Zan | Ranitidine Hydrochloride Tablets 150mg |
| 0363-0362 | Wal-Zan | Ranitidine |
| 0363-1029 | Wal-Zan | Wal-Zan |
| 0363-1030 | Wal-Zan | Wal-Zan |
| 21130-404 | Acid Reducer 150 | Ranitidine Hydrochloride Tablets 150mg |
| 49035-404 | Ranitidine 150 | Ranitidine Hydrochloride Tablets 150mg |
| 69168-375 | Ranitidine 150 | Ranitidine Hydrochloride Tablets 150mg |
| 69168-389 | Ranitidine 150 | Ranitidine Hydrochloride Tablets 150mg |
Trademark Results [Wal-Zan]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 WAL-ZAN 76669853 3281366 Live/Registered |
WALGREEN CO. 2006-12-04 |
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