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DOXYCYCLINE
DOXYCYCLINE - 68180-657-01 - (DOXYCYCLINE)
Drug Information of DOXYCYCLINE
| Product NDC: | 68180-657 |
| Proprietary Name: | DOXYCYCLINE |
| Non Proprietary Name: | DOXYCYCLINE |
| Active Ingredient(s): | 25 mg/5mL & nbsp; DOXYCYCLINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DOXYCYCLINE
| Product NDC: | 68180-657 |
| Labeler Name: | Lupin Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201678 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130604 |
Package Information of DOXYCYCLINE
| Package NDC: | 68180-657-01 |
| Package Description: | 60 mL in 1 BOTTLE (68180-657-01) |
NDC Information of DOXYCYCLINE
| NDC Code | 68180-657-01 |
| Proprietary Name | DOXYCYCLINE |
| Package Description | 60 mL in 1 BOTTLE (68180-657-01) |
| Product NDC | 68180-657 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DOXYCYCLINE |
| Dosage Form Name | FOR SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20130604 |
| Marketing Category Name | ANDA |
| Labeler Name | Lupin Pharmaceuticals, Inc. |
| Substance Name | DOXYCYCLINE |
| Strength Number | 25 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
