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Doxycycline
Doxycycline - 55390-110-10 - (Doxycycline)
Drug Information of Doxycycline
| Product NDC: | 55390-110 |
| Proprietary Name: | Doxycycline |
| Non Proprietary Name: | Doxycycline |
| Active Ingredient(s): | 100 mg/10mL & nbsp; Doxycycline |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Doxycycline
| Product NDC: | 55390-110 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062569 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20011001 |
Package Information of Doxycycline
| Package NDC: | 55390-110-10 |
| Package Description: | 10 VIAL in 1 BOX (55390-110-10) > 10 mL in 1 VIAL |
NDC Information of Doxycycline
| NDC Code | 55390-110-10 |
| Proprietary Name | Doxycycline |
| Package Description | 10 VIAL in 1 BOX (55390-110-10) > 10 mL in 1 VIAL |
| Product NDC | 55390-110 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Doxycycline |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20011001 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | DOXYCYCLINE HYCLATE |
| Strength Number | 100 |
| Strength Unit | mg/10mL |
| Pharmaceutical Classes | Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient] |
