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DOXYCYCLINE
DOXYCYCLINE - 23155-133-01 - (DOXYCYCLINE)
Drug Information of DOXYCYCLINE
| Product NDC: | 23155-133 |
| 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: | 23155-133 |
| Labeler Name: | Heritage Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091605 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120105 |
Package Information of DOXYCYCLINE
| Package NDC: | 23155-133-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (23155-133-01) |
NDC Information of DOXYCYCLINE
| NDC Code | 23155-133-01 |
| Proprietary Name | DOXYCYCLINE |
| Package Description | 100 TABLET in 1 BOTTLE (23155-133-01) |
| Product NDC | 23155-133 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DOXYCYCLINE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120105 |
| Marketing Category Name | ANDA |
| Labeler Name | Heritage Pharmaceuticals Inc. |
| Substance Name | DOXYCYCLINE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
