| 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 |