Doxycycline Hyclate
- Product NDC
- 51862-709
- 11-digit product format
- 518620709
- Labeler code
- 51862
- Product ID
- 51862-709_b6329a99-ca11-4da2-845e-eafa14443468
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Mayne Pharma
- Application
- NDA050795
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2016-05-26
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC], Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51862-709 | DOXYCYCLINE HYCLATE TABLET, DELAYED RELEASE [MAYNE PHARMA COMMERCIAL LLC] | 11 | Legacy NDC | 20250418_f9c63af9-d613-43fc-b8e5-ab6219f24c70.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51862-709-12 | 51862070912 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (51862-709-12) | 2016-05-26 | 0000-00-00 | No | No | Current |