Product NDC: | 0069-0970 |
Proprietary Name: | Vibramycin Monohydrate |
Non Proprietary Name: | DOXYCYCLINE |
Active Ingredient(s): | 25 mg/5mL & nbsp; DOXYCYCLINE |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER, FOR SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0069-0970 |
Labeler Name: | Pfizer Laboratories Div Pfizer Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA050006 |
Marketing Category: | NDA |
Start Marketing Date: | 19671206 |
Package NDC: | 0069-0970-65 |
Package Description: | 60 mL in 1 BOTTLE (0069-0970-65) |
NDC Code | 0069-0970-65 |
Proprietary Name | Vibramycin Monohydrate |
Package Description | 60 mL in 1 BOTTLE (0069-0970-65) |
Product NDC | 0069-0970 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | DOXYCYCLINE |
Dosage Form Name | POWDER, FOR SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 19671206 |
Marketing Category Name | NDA |
Labeler Name | Pfizer Laboratories Div Pfizer Inc |
Substance Name | DOXYCYCLINE |
Strength Number | 25 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |