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Cimetidine
Cimetidine - 0409-7444-01 - (CIMETIDINE HYDROCHLORIDE)
Drug Information of Cimetidine
| Product NDC: | 0409-7444 |
| Proprietary Name: | Cimetidine |
| Non Proprietary Name: | CIMETIDINE HYDROCHLORIDE |
| Active Ingredient(s): | 150 mg/mL & nbsp; CIMETIDINE HYDROCHLORIDE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cimetidine
| Product NDC: | 0409-7444 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074344 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110708 |
Package Information of Cimetidine
| Package NDC: | 0409-7444-01 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-7444-01) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Cimetidine
| NDC Code | 0409-7444-01 |
| Proprietary Name | Cimetidine |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-7444-01) > 2 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0409-7444 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CIMETIDINE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20110708 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | CIMETIDINE HYDROCHLORIDE |
| Strength Number | 150 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |
