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Doxycycline
Doxycycline - 0069-0104-04 - (DOXYCYCLINE HYCLATE)
Drug Information of Doxycycline
| Product NDC: | 0069-0104 |
| Proprietary Name: | Doxycycline |
| Non Proprietary Name: | DOXYCYCLINE HYCLATE |
| Active Ingredient(s): | 100 mg/10mL & nbsp; DOXYCYCLINE HYCLATE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Doxycycline
| Product NDC: | 0069-0104 |
| Labeler Name: | Pfizer Laboratories Div Pfizer Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091406 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120821 |
Package Information of Doxycycline
| Package NDC: | 0069-0104-04 |
| Package Description: | 10 VIAL in 1 CARTON (0069-0104-04) > 10 mL in 1 VIAL (0069-0104-01) |
NDC Information of Doxycycline
| NDC Code | 0069-0104-04 |
| Proprietary Name | Doxycycline |
| Package Description | 10 VIAL in 1 CARTON (0069-0104-04) > 10 mL in 1 VIAL (0069-0104-01) |
| Product NDC | 0069-0104 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DOXYCYCLINE HYCLATE |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20120821 |
| Marketing Category Name | ANDA |
| Labeler Name | Pfizer Laboratories Div Pfizer Inc |
| Substance Name | DOXYCYCLINE HYCLATE |
| Strength Number | 100 |
| Strength Unit | mg/10mL |
| Pharmaceutical Classes |
