| Product NDC: | 50383-050 |
| Proprietary Name: | Cimetidine Hydrochloride Oral Solution |
| Non Proprietary Name: | Cimetidine Hydrochloride Oral Solution |
| Active Ingredient(s): | 300 mg/5mL & nbsp; Cimetidine Hydrochloride Oral Solution |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50383-050 |
| Labeler Name: | Hi-Tech Pharmacal Co., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074664 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19971028 |
| Package NDC: | 50383-050-08 |
| Package Description: | 237 mL in 1 BOTTLE (50383-050-08) |
| NDC Code | 50383-050-08 |
| Proprietary Name | Cimetidine Hydrochloride Oral Solution |
| Package Description | 237 mL in 1 BOTTLE (50383-050-08) |
| Product NDC | 50383-050 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cimetidine Hydrochloride Oral Solution |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19971028 |
| Marketing Category Name | ANDA |
| Labeler Name | Hi-Tech Pharmacal Co., Inc. |
| Substance Name | CIMETIDINE HYDROCHLORIDE |
| Strength Number | 300 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |