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Doxycycline Hyclate
Doxycycline Hyclate - 0172-4626-70 - (Doxycycline Hyclate)
Drug Information of Doxycycline Hyclate
| Product NDC: | 0172-4626 |
| Proprietary Name: | Doxycycline Hyclate |
| Non Proprietary Name: | Doxycycline Hyclate |
| Active Ingredient(s): | 20 mg/1 & nbsp; Doxycycline Hyclate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Doxycycline Hyclate
| Product NDC: | 0172-4626 |
| Labeler Name: | IVAX Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065163 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050517 |
Package Information of Doxycycline Hyclate
| Package NDC: | 0172-4626-70 |
| Package Description: | 500 TABLET, FILM COATED in 1 BOTTLE (0172-4626-70) |
NDC Information of Doxycycline Hyclate
| NDC Code | 0172-4626-70 |
| Proprietary Name | Doxycycline Hyclate |
| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (0172-4626-70) |
| Product NDC | 0172-4626 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Doxycycline Hyclate |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20050517 |
| Marketing Category Name | ANDA |
| Labeler Name | IVAX Pharmaceuticals, Inc. |
| Substance Name | DOXYCYCLINE HYCLATE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
