Doxycycline
- Product NDC
- 50090-5983
- 11-digit product format
- 500905983
- Labeler code
- 50090
- Product ID
- 50090-5983_b7c64de0-efcd-4fcf-8f5b-29133a9e916d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA204446
- Marketing category
- ANDA
- Marketing start
- 2015-05-28
- 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
- 2023-12-31
- 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 |
|---|
| 50090-5983-0 | 50090598300 | 20 CAPSULE in 1 BOTTLE (50090-5983-0) | 20 capsule | 2022-05-26 | 0000-00-00 | No | No | Current |
| 50090-5983-1 | 50090598301 | 14 CAPSULE in 1 BOTTLE (50090-5983-1) | 14 capsule | 2022-06-01 | 0000-00-00 | No | No | Current |