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Ranitidine
Ranitidine - 59726-580-10 - (Ranitidine)
Drug Information of Ranitidine
| Product NDC: | 59726-580 |
| Proprietary Name: | Ranitidine |
| Non Proprietary Name: | Ranitidine |
| Active Ingredient(s): | 75 mg/1 & nbsp; Ranitidine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ranitidine
| Product NDC: | 59726-580 |
| Labeler Name: | P and L Development of New York Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA078884 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130319 |
Package Information of Ranitidine
| Package NDC: | 59726-580-10 |
| Package Description: | 1 BOTTLE in 1 BOX (59726-580-10) > 10 TABLET in 1 BOTTLE |
NDC Information of Ranitidine
| NDC Code | 59726-580-10 |
| Proprietary Name | Ranitidine |
| Package Description | 1 BOTTLE in 1 BOX (59726-580-10) > 10 TABLET in 1 BOTTLE |
| Product NDC | 59726-580 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ranitidine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130319 |
| Marketing Category Name | ANDA |
| Labeler Name | P and L Development of New York Corporation |
| Substance Name | RANITIDINE HYDROCHLORIDE |
| Strength Number | 75 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
