Product NDC: | 0069-0990 |
Proprietary Name: | Vibra-Tabs |
Non Proprietary Name: | DOXYCYCLINE HYCLATE |
Active Ingredient(s): | 100 mg/1 & nbsp; DOXYCYCLINE HYCLATE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0069-0990 |
Labeler Name: | Pfizer Laboratories Div Pfizer Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA050533 |
Marketing Category: | NDA |
Start Marketing Date: | 19800115 |
Package NDC: | 0069-0990-50 |
Package Description: | 50 TABLET, FILM COATED in 1 BOTTLE (0069-0990-50) |
NDC Code | 0069-0990-50 |
Proprietary Name | Vibra-Tabs |
Package Description | 50 TABLET, FILM COATED in 1 BOTTLE (0069-0990-50) |
Product NDC | 0069-0990 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | DOXYCYCLINE HYCLATE |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 19800115 |
Marketing Category Name | NDA |
Labeler Name | Pfizer Laboratories Div Pfizer Inc |
Substance Name | DOXYCYCLINE HYCLATE |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes |