DOXYCYCLINE HYCLATE
- Product NDC
- 61919-667
- 11-digit product format
- 619190667
- Labeler code
- 61919
- Product ID
- 61919-667_94e15996-1873-0961-e053-2995a90a042f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DOXYCYCLINE HYCLATE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA062505
- Marketing category
- ANDA
- Marketing start
- 2019-09-10
- 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
- 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 |
|---|
| 61919-667-14 | 61919066714 | 14 TABLET, FILM COATED in 1 BOTTLE (61919-667-14) | 2019-09-10 | 0000-00-00 | No | No | Current |
| 61919-667-20 | 61919066720 | 20 TABLET, FILM COATED in 1 BOTTLE (61919-667-20) | 2019-09-10 | 0000-00-00 | No | No | Current |