| 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 |