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Cimetidine Hydrochloride
Cimetidine Hydrochloride - 60432-007-08 - (Cimetidine Hydrochloride)
Drug Information of Cimetidine Hydrochloride
| Product NDC: | 60432-007 |
| Proprietary Name: | Cimetidine Hydrochloride |
| Non Proprietary Name: | Cimetidine Hydrochloride |
| Active Ingredient(s): | 300 mg/5mL & nbsp; Cimetidine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cimetidine Hydrochloride
| Product NDC: | 60432-007 |
| Labeler Name: | Morton Grove Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074757 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19970312 |
Package Information of Cimetidine Hydrochloride
| Package NDC: | 60432-007-08 |
| Package Description: | 237 mL in 1 BOTTLE (60432-007-08) |
NDC Information of Cimetidine Hydrochloride
| NDC Code | 60432-007-08 |
| Proprietary Name | Cimetidine Hydrochloride |
| Package Description | 237 mL in 1 BOTTLE (60432-007-08) |
| Product NDC | 60432-007 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cimetidine Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19970312 |
| Marketing Category Name | ANDA |
| Labeler Name | Morton Grove Pharmaceuticals, Inc. |
| Substance Name | CIMETIDINE HYDROCHLORIDE |
| Strength Number | 300 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |
