doxycycline is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Zydus Pharmaceuticals (usa) Inc.. The primary component is Doxycycline.
| Product ID | 68382-782_632bd3a7-811e-42f7-ae56-308a81fd5885 |
| NDC | 68382-782 |
| Product Type | Human Prescription Drug |
| Proprietary Name | doxycycline |
| Generic Name | Doxycycline |
| Dosage Form | Capsule |
| Route of Administration | ORAL |
| Marketing Start Date | 2016-03-14 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA205115 |
| Labeler Name | Zydus Pharmaceuticals (USA) Inc. |
| Substance Name | DOXYCYCLINE |
| Active Ingredient Strength | 50 mg/1 |
| Pharm Classes | Tetracycline-class Drug [EPC],Tetracyclines [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2016-03-14 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA205115 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-03-14 |
| Marketing Category | ANDA |
| Application Number | ANDA205115 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-03-14 |
| Marketing Category | ANDA |
| Application Number | ANDA205115 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-03-14 |
| Marketing Category | ANDA |
| Application Number | ANDA205115 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-03-14 |
| Marketing Category | ANDA |
| Application Number | ANDA205115 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-03-14 |
| Marketing Category | ANDA |
| Application Number | ANDA205115 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-03-14 |
| Marketing Category | ANDA |
| Application Number | ANDA205115 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-03-14 |
| Marketing Category | ANDA |
| Application Number | ANDA205115 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-03-14 |
| Ingredient | Strength |
|---|---|
| DOXYCYCLINE | 50 mg/1 |
| SPL SET ID: | fef9580d-8850-4cbb-89eb-2b4d40ee59c9 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| PHarm Class EPC | |
| NUI Code |