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Aprodine
Aprodine - 21695-929-60 - (Pseudoephedrine HCl and Tripolidine)
Drug Information of Aprodine
| Product NDC: | 21695-929 |
| Proprietary Name: | Aprodine |
| Non Proprietary Name: | Pseudoephedrine HCl and Tripolidine |
| Active Ingredient(s): | 60; 2.5 mg/1; mg/1 & nbsp; Pseudoephedrine HCl and Tripolidine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aprodine
| Product NDC: | 21695-929 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19930109 |
Package Information of Aprodine
| Package NDC: | 21695-929-60 |
| Package Description: | 60 TABLET, FILM COATED in 1 BOTTLE (21695-929-60) |
NDC Information of Aprodine
| NDC Code | 21695-929-60 |
| Proprietary Name | Aprodine |
| Package Description | 60 TABLET, FILM COATED in 1 BOTTLE (21695-929-60) |
| Product NDC | 21695-929 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pseudoephedrine HCl and Tripolidine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19930109 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE |
| Strength Number | 60; 2.5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
