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doxycycline
doxycycline - 0185-0106-05 - (doxycycline)
Drug Information of doxycycline
| Product NDC: | 0185-0106 |
| Proprietary Name: | doxycycline |
| Non Proprietary Name: | doxycycline |
| Active Ingredient(s): | 75 mg/1 & nbsp; doxycycline |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of doxycycline
| Product NDC: | 0185-0106 |
| Labeler Name: | Eon Labs, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065353 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20061127 |
Package Information of doxycycline
| Package NDC: | 0185-0106-05 |
| Package Description: | 500 TABLET, FILM COATED in 1 BOTTLE (0185-0106-05) |
NDC Information of doxycycline
| NDC Code | 0185-0106-05 |
| Proprietary Name | doxycycline |
| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (0185-0106-05) |
| Product NDC | 0185-0106 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | doxycycline |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20061127 |
| Marketing Category Name | ANDA |
| Labeler Name | Eon Labs, Inc. |
| Substance Name | DOXYCYCLINE |
| Strength Number | 75 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
