Product NDC: | 68788-0446 |
Proprietary Name: | AK-Con |
Non Proprietary Name: | naphazoline hydrochloride |
Active Ingredient(s): | 1 mg/mL & nbsp; naphazoline hydrochloride |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68788-0446 |
Labeler Name: | Preferred Pharmaceuticals, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA083590 |
Marketing Category: | ANDA |
Start Marketing Date: | 19740822 |
Package NDC: | 68788-0446-1 |
Package Description: | 15 mL in 1 BOTTLE, PLASTIC (68788-0446-1) |
NDC Code | 68788-0446-1 |
Proprietary Name | AK-Con |
Package Description | 15 mL in 1 BOTTLE, PLASTIC (68788-0446-1) |
Product NDC | 68788-0446 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | naphazoline hydrochloride |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 19740822 |
Marketing Category Name | ANDA |
Labeler Name | Preferred Pharmaceuticals, Inc |
Substance Name | NAPHAZOLINE HYDROCHLORIDE |
Strength Number | 1 |
Strength Unit | mg/mL |
Pharmaceutical Classes |