Doxycycline
- Product NDC
- 55700-122
- 11-digit product format
- 557000122
- Labeler code
- 55700
- Product ID
- 55700-122_70cb44cc-de5b-4ed6-a49c-08038d05d1a7
- 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
- 100 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-122-20 | 55700012220 | 20 TABLET in 1 BOTTLE (55700-122-20) | 20 tablet | 2012-01-05 | 0000-00-00 | No | No | Current |