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Ranitidine Hydrochloride
Ranitidine Hydrochloride - 55111-404-62 - (Ranitidine Hydrochloride)
Drug Information of Ranitidine Hydrochloride
| Product NDC: | 55111-404 |
| Proprietary Name: | Ranitidine Hydrochloride |
| Non Proprietary Name: | Ranitidine Hydrochloride |
| Active Ingredient(s): | 168 mg/1 & nbsp; Ranitidine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ranitidine Hydrochloride
| Product NDC: | 55111-404 |
| Labeler Name: | Dr. Reddy's Laboratories Limited |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA078192 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091202 |
Package Information of Ranitidine Hydrochloride
| Package NDC: | 55111-404-62 |
| Package Description: | 1 BOTTLE in 1 CARTON (55111-404-62) > 95 TABLET, COATED in 1 BOTTLE |
NDC Information of Ranitidine Hydrochloride
| NDC Code | 55111-404-62 |
| Proprietary Name | Ranitidine Hydrochloride |
| Package Description | 1 BOTTLE in 1 CARTON (55111-404-62) > 95 TABLET, COATED in 1 BOTTLE |
| Product NDC | 55111-404 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ranitidine Hydrochloride |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20091202 |
| Marketing Category Name | ANDA |
| Labeler Name | Dr. Reddy's Laboratories Limited |
| Substance Name | RANITIDINE HYDROCHLORIDE |
| Strength Number | 168 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
