Product NDC: | 0069-0971 |
Proprietary Name: | Vibramycin Calcium |
Non Proprietary Name: | DOXYCYCLINE CALCIUM |
Active Ingredient(s): | 50 mg/5mL & nbsp; DOXYCYCLINE CALCIUM |
Administration Route(s): | ORAL |
Dosage Form(s): | SYRUP |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0069-0971 |
Labeler Name: | Pfizer Laboratories Div Pfizer Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA050480 |
Marketing Category: | NDA |
Start Marketing Date: | 19740923 |
Package NDC: | 0069-0971-93 |
Package Description: | 473 mL in 1 BOTTLE (0069-0971-93) |
NDC Code | 0069-0971-93 |
Proprietary Name | Vibramycin Calcium |
Package Description | 473 mL in 1 BOTTLE (0069-0971-93) |
Product NDC | 0069-0971 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | DOXYCYCLINE CALCIUM |
Dosage Form Name | SYRUP |
Route Name | ORAL |
Start Marketing Date | 19740923 |
Marketing Category Name | NDA |
Labeler Name | Pfizer Laboratories Div Pfizer Inc |
Substance Name | DOXYCYCLINE CALCIUM |
Strength Number | 50 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |