Doxycycline Hyclate
- Product NDC
- 51862-696
- 11-digit product format
- 518620696
- Labeler code
- 51862
- Product ID
- 51862-696_b7a12bb2-6295-4722-bf1b-d9b5aec3326c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mayne Pharma Inc.
- Application
- ANDA208765
- Marketing category
- ANDA
- Marketing start
- 2017-06-14
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 51862-696-06 | 51862069606 | 60 TABLET, FILM COATED in 1 BOTTLE (51862-696-06) | 2017-06-14 | 0000-00-00 | No | No | Current |