Doxycycline
- Product NDC
- 55700-086
- 11-digit product format
- 557000086
- Labeler code
- 55700
- Product ID
- 55700-086_cf73d903-cd80-4de4-9c14-871566e200c4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA091605
- Marketing category
- ANDA
- Marketing start
- 2012-01-05
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE
- Active strength
- 50 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| N12000U13O | DOXYCYCLINE | 17086-28-1 | DOXYCYCLINE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-086-28 | 55700008628 | 28 TABLET in 1 BOTTLE (55700-086-28) | 28 tablet | 2012-01-05 | 0000-00-00 | No | No | Current |
| 55700-086-30 | 55700008630 | 30 TABLET in 1 BOTTLE (55700-086-30) | 30 tablet | 2012-01-05 | 0000-00-00 | No | No | Current |