Doxycycline Hyclate
- Product NDC
- 50090-3860
- 11-digit product format
- 500903860
- Labeler code
- 50090
- Product ID
- 50090-3860_0883c745-af10-4eb5-8815-b5f15eca8aa3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA062505
- Marketing category
- ANDA
- Marketing start
- 1984-09-11
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3860-6 | 50090386006 | 2 TABLET, FILM COATED in 1 BOTTLE (50090-3860-6) | 2018-11-26 | 0000-00-00 | No | No | Current |