Doxycycline Hyclate
- Product NDC
- 46708-352
- 11-digit product format
- 467080352
- Labeler code
- 46708
- Product ID
- 46708-352_994cfe3e-3b42-4837-b9fc-c88ba7484e51
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Alembic Pharmaceuticals Limited
- Application
- ANDA210537
- Marketing category
- ANDA
- Marketing start
- 2020-03-05
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 20 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 |
|---|
| 46708-352-31 | 46708035231 | 100 TABLET, FILM COATED in 1 BOTTLE (46708-352-31) | 2020-03-05 | No | No | Historical |
| 46708-352-60 | 46708035260 | 60 TABLET, FILM COATED in 1 BOTTLE (46708-352-60) | 2020-03-05 | No | No | Historical |
| 46708-352-91 | 46708035291 | 1000 TABLET, FILM COATED in 1 BOTTLE (46708-352-91) | 2020-03-05 | No | No | Historical |