doxycycline hyclate
- Product NDC
- 71335-2844
- 11-digit product format
- 713352844
- Labeler code
- 71335
- Product ID
- 71335-2844_3e71b6ff-d53a-438e-8b76-e63b712e2cc2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- doxycycline hyclate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA062500
- Marketing category
- ANDA
- Marketing start
- 1984-09-11
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 50 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 |
|---|
| 19XTS3T51U | DOXYCYCLINE HYCLATE | 24390-14-5 | DOXYCYCLINE HYCLATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2844-1 | 71335284401 | 50 CAPSULE in 1 BOTTLE (71335-2844-1) | 50 capsule | 2025-10-30 | No | No | Historical |