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ZANTAC
ZANTAC - 0173-0363-00 - (ranitidine hydrochloride)
Drug Information of ZANTAC
| Product NDC: | 0173-0363 |
| Proprietary Name: | ZANTAC |
| Non Proprietary Name: | ranitidine hydrochloride |
| Active Ingredient(s): | 25 mg/mL & nbsp; ranitidine hydrochloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ZANTAC
| Product NDC: | 0173-0363 |
| Labeler Name: | GlaxoSmithKline LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019090 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19891001 |
Package Information of ZANTAC
| Package NDC: | 0173-0363-00 |
| Package Description: | 40 mL in 1 VIAL, PHARMACY BULK PACKAGE (0173-0363-00) |
NDC Information of ZANTAC
| NDC Code | 0173-0363-00 |
| Proprietary Name | ZANTAC |
| Package Description | 40 mL in 1 VIAL, PHARMACY BULK PACKAGE (0173-0363-00) |
| Product NDC | 0173-0363 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ranitidine hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19891001 |
| Marketing Category Name | NDA |
| Labeler Name | GlaxoSmithKline LLC |
| Substance Name | RANITIDINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |
