Doxycycline Hyclate
- Product NDC
- 50090-7800
- 11-digit product format
- 500907800
- Labeler code
- 50090
- Product ID
- 50090-7800_198523f1-ce8e-42b5-adfe-6ebf3e78cdc3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA062269
- Marketing category
- ANDA
- Marketing start
- 2025-03-07
- 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7800-0 | 50090780000 | 20 TABLET, FILM COATED in 1 BOTTLE (50090-7800-0) | 2025-11-25 | No | No | Historical |