Doxycycline
- Product NDC
- 68071-3752
- 11-digit product format
- 680713752
- Labeler code
- 68071
- Product ID
- 68071-3752_2a0a0cbe-2751-78fb-e063-6294a90a39c6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA209165
- Marketing category
- ANDA
- Marketing start
- 2017-07-31
- Substance
- DOXYCYCLINE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC], Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 68071-3752-2 | 68071375202 | 20 CAPSULE in 1 BOTTLE (68071-3752-2) | 20 capsule | 2024-12-24 | No | No | Historical |
| 68071-3752-4 | 68071375204 | 14 CAPSULE in 1 BOTTLE (68071-3752-4) | 14 capsule | 2024-12-24 | No | No | Historical |