Doxycycline
- Product NDC
- 51862-041
- 11-digit product format
- 518620041
- Labeler code
- 51862
- Product ID
- 51862-041_f864b33a-9861-491a-a6b1-e02992df0950
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Mayne Pharma Inc.
- Application
- ANDA209396
- Marketing category
- ANDA
- Marketing start
- 2018-03-09
- Marketing end
- 2022-03-31
- Substance
- DOXYCYCLINE
- Active strength
- 75 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 51862-041-01 | 51862004101 | 100 CAPSULE in 1 BOTTLE (51862-041-01) | 100 capsule | 2018-03-09 | 0000-00-00 | No | No | Current |