Doxycycline
- Product NDC
- 50090-1472
- 11-digit product format
- 500901472
- Labeler code
- 50090
- Product ID
- 50090-1472_f341cd99-e0a4-4c2d-a351-b49f5f2fc982
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- doxycycline
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065055
- Marketing category
- ANDA
- Marketing start
- 2000-12-01
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| N12000U13O | DOXYCYCLINE | 17086-28-1 | DOXYCYCLINE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1472-0 | 50090147200 | 20 CAPSULE in 1 BOTTLE (50090-1472-0) | 20 capsule | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-1472-1 | 50090147201 | 14 CAPSULE in 1 BOTTLE (50090-1472-1) | 14 capsule | 2019-02-07 | 0000-00-00 | No | No | Current |