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Doxycycline
Doxycycline - 49884-091-01 - (doxycycline)
Drug Information of Doxycycline
| Product NDC: | 49884-091 |
| Proprietary Name: | Doxycycline |
| Non Proprietary Name: | doxycycline |
| Active Ingredient(s): | 50 mg/1 & nbsp; doxycycline |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Doxycycline
| Product NDC: | 49884-091 |
| Labeler Name: | Par Pharmaceutical Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065070 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20001215 |
Package Information of Doxycycline
| Package NDC: | 49884-091-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (49884-091-01) |
NDC Information of Doxycycline
| NDC Code | 49884-091-01 |
| Proprietary Name | Doxycycline |
| Package Description | 100 TABLET in 1 BOTTLE (49884-091-01) |
| Product NDC | 49884-091 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | doxycycline |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20001215 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical Inc |
| Substance Name | DOXYCYCLINE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
