DOXYCYCLINE HYCLATE
- Product NDC
- 82804-070
- 11-digit product format
- 828040070
- Labeler code
- 82804
- Product ID
- 82804-070_e38f3cd2-47e5-438f-bbe3-50b578360f74
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DOXYCYCLINE HYCLATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA211343
- Marketing category
- ANDA
- Marketing start
- 2019-10-09
- Substance
- DOXYCYCLINE HYCLATE
- 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 |
|---|
| 19XTS3T51U | DOXYCYCLINE HYCLATE | 24390-14-5 | DOXYCYCLINE HYCLATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-070-14 | 82804007014 | 14 TABLET in 1 BOTTLE (82804-070-14) | 14 tablet | 2024-03-21 | No | No | Historical |