Product NDC: | 68094-316 |
Proprietary Name: | Ranitidine Hydrochloride |
Non Proprietary Name: | Ranitidine Hydrochloride |
Active Ingredient(s): | 15 mg/mL & nbsp; Ranitidine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68094-316 |
Labeler Name: | Precision Dose Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078312 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110425 |
Package NDC: | 68094-316-58 |
Package Description: | 50 BAG in 1 CASE (68094-316-58) > 1 SYRINGE, PLASTIC in 1 BAG > 1 mL in 1 SYRINGE, PLASTIC |
NDC Code | 68094-316-58 |
Proprietary Name | Ranitidine Hydrochloride |
Package Description | 50 BAG in 1 CASE (68094-316-58) > 1 SYRINGE, PLASTIC in 1 BAG > 1 mL in 1 SYRINGE, PLASTIC |
Product NDC | 68094-316 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ranitidine Hydrochloride |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20110425 |
Marketing Category Name | ANDA |
Labeler Name | Precision Dose Inc. |
Substance Name | RANITIDINE HYDROCHLORIDE |
Strength Number | 15 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |