Doxycycline Monohydrate is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Doxycycline.
| Product ID | 63629-5361_ab5207ff-53ed-425b-9ef7-b8a56d411225 |
| NDC | 63629-5361 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Doxycycline Monohydrate |
| Generic Name | Doxycycline |
| Dosage Form | Capsule |
| Route of Administration | ORAL |
| Marketing Start Date | 2005-02-07 |
| Marketing Category | NDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC |
| Application Number | NDA050641 |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | DOXYCYCLINE |
| Active Ingredient Strength | 100 mg/1 |
| Pharm Classes | Tetracycline-class Drug [EPC],Tetracyclines [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2014-06-16 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA050641 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-03-31 |
| Marketing End Date | 2019-03-31 |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA050641 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-03-31 |
| Marketing End Date | 2019-03-31 |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA050641 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-03-31 |
| Marketing End Date | 2019-03-31 |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA050641 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-03-31 |
| Marketing End Date | 2019-03-31 |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA050641 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-03-31 |
| Marketing End Date | 2019-03-31 |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA050641 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-03-31 |
| Marketing End Date | 2019-03-31 |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA050641 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-03-31 |
| Marketing End Date | 2019-03-31 |
| Ingredient | Strength |
|---|---|
| DOXYCYCLINE | 100 mg/1 |
| SPL SET ID: | 78234a1c-5728-4bbc-9128-7301c9d804be |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| PHarm Class EPC | |
| NUI Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0591-0411 | Doxycycline Monohydrate | Doxycycline Monohydrate |
| 0591-0410 | Doxycycline Monohydrate | Doxycycline Monohydrate |
| 0591-2404 | Doxycycline Monohydrate | Doxycycline Monohydrate |
| 71610-220 | Doxycycline Monohydrate | Doxycycline Monohydrate |
| 43063-529 | Doxycycline Monohydrate | Doxycycline Monohydrate |
| 43063-789 | Doxycycline Monohydrate | Doxycycline Monohydrate |
| 63629-5361 | Doxycycline Monohydrate | Doxycycline Monohydrate |
| 67296-1578 | Doxycycline Monohydrate | Doxycycline Monohydrate |
| 61919-624 | DOXYCYCLINE MONOHYDRATE | DOXYCYCLINE MONOHYDRATE |
| 53002-0671 | Doxycycline Monohydrate | Doxycycline Monohydrate |
| 0115-1327 | Doxycycline | Doxycycline |
| 0143-9381 | Doxycycline | Doxycycline |
| 0179-0129 | Doxycycline | Doxycycline |
| 0378-5475 | Doxycycline | doxycycline |
| 0378-6021 | Doxycycline | Doxycycline |
| 0378-6022 | Doxycycline | Doxycycline |
| 0378-6023 | Doxycycline | Doxycycline |
| 0378-6124 | Doxycycline | Doxycycline |
| 0404-9855 | DOXYCYCLINE | doxycycline |
| 0527-1335 | Doxycycline | Doxycycline |
| 0527-1338 | Doxycycline | Doxycycline |
| 0527-1535 | Doxycycline | Doxycycline |
| 0527-1537 | Doxycycline | Doxycycline |
| 0378-0145 | doxycycline hyclate | doxycycline |
| 0378-0148 | doxycycline hyclate | doxycycline |
| 0378-0167 | doxycycline hyclate | doxycycline |
| 0299-3822 | ORACEA | DOXYCYCLINE |
| 0069-0970 | Vibramycin Monohydrate | doxycycline |