Doxycycline Hyclate
- Product NDC
- 23155-376
- 11-digit product format
- 231550376
- Labeler code
- 23155
- Product ID
- 23155-376_428abb4d-c537-4c52-b3c2-b236c6120c81
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Heritage Pharmaceuticals Inc.
- Application
- ANDA209969
- Marketing category
- ANDA
- Marketing start
- 2018-12-01
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 100 1/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 23155-376-01 | 23155037601 | 100 TABLET, FILM COATED in 1 BOTTLE (23155-376-01) | 2018-12-01 | 0000-00-00 | No | No | Current |
| 23155-376-05 | 23155037605 | 500 TABLET, FILM COATED in 1 BOTTLE (23155-376-05) | 2018-12-01 | 0000-00-00 | No | No | Current |
| 23155-376-25 | 23155037625 | 50 TABLET, FILM COATED in 1 BOTTLE (23155-376-25) | 2018-12-01 | 0000-00-00 | No | No | Current |