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ATRIDOX
ATRIDOX - 63646-191-03 - (Doxycycline Hyclate)
Drug Information of ATRIDOX
| Product NDC: | 63646-191 |
| Proprietary Name: | ATRIDOX |
| Non Proprietary Name: | Doxycycline Hyclate |
| Active Ingredient(s): | & nbsp; Doxycycline Hyclate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ATRIDOX
| Product NDC: | 63646-191 |
| Labeler Name: | TOLMAR Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050751 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19980903 |
Package Information of ATRIDOX
| Package NDC: | 63646-191-03 |
| Package Description: | 2 TRAY in 1 CARTON (63646-191-03) > 1 KIT in 1 TRAY (63646-191-06) * 50 mg in 1 SYRINGE (63646-193-08) * 450 mg in 1 SYRINGE (63646-192-07) |
NDC Information of ATRIDOX
| NDC Code | 63646-191-03 |
| Proprietary Name | ATRIDOX |
| Package Description | 2 TRAY in 1 CARTON (63646-191-03) > 1 KIT in 1 TRAY (63646-191-06) * 50 mg in 1 SYRINGE (63646-193-08) * 450 mg in 1 SYRINGE (63646-192-07) |
| Product NDC | 63646-191 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Doxycycline Hyclate |
| Dosage Form Name | KIT |
| Route Name | ORAL |
| Start Marketing Date | 19980903 |
| Marketing Category Name | NDA |
| Labeler Name | TOLMAR Inc. |
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