Doxycycline
- Product NDC
- 68071-2152
- 11-digit product format
- 680712152
- Labeler code
- 68071
- Product ID
- 68071-2152_10f5738a-b59d-0767-e063-6294a90ada33
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- doxycycline
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA065055
- Marketing category
- ANDA
- Marketing start
- 2022-08-01
- 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 |
|---|
| 68071-2152-2 | 68071215202 | 20 CAPSULE in 1 BOTTLE (68071-2152-2) | 20 capsule | 2023-04-24 | No | No | Historical |
| 68071-2152-4 | 68071215204 | 14 CAPSULE in 1 BOTTLE (68071-2152-4) | 14 capsule | 2023-04-24 | No | No | Historical |