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Doxycycline
Doxycycline - 24658-220-20 - (Doxycycline hyclate)
Drug Information of Doxycycline
| Product NDC: | 24658-220 |
| Proprietary Name: | Doxycycline |
| Non Proprietary Name: | Doxycycline hyclate |
| Active Ingredient(s): | 100 mg/1 & nbsp; Doxycycline hyclate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Doxycycline
| Product NDC: | 24658-220 |
| Labeler Name: | Blu Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065095 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100501 |
Package Information of Doxycycline
| Package NDC: | 24658-220-20 |
| Package Description: | 20 TABLET, COATED in 1 BOTTLE (24658-220-20) |
NDC Information of Doxycycline
| NDC Code | 24658-220-20 |
| Proprietary Name | Doxycycline |
| Package Description | 20 TABLET, COATED in 1 BOTTLE (24658-220-20) |
| Product NDC | 24658-220 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Doxycycline hyclate |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100501 |
| Marketing Category Name | ANDA |
| Labeler Name | Blu Pharmaceuticals, LLC |
| Substance Name | DOXYCYCLINE HYCLATE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
