Doxycycline
- Product NDC
- 51862-042
- 11-digit product format
- 518620042
- Labeler code
- 51862
- Product ID
- 51862-042_00a173d0-5583-4d2f-a74e-f756e310c93f
- 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
- 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
- 2022-12-31
- 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 |
|---|
| 51862-042-02 | 51862004202 | 250 CAPSULE in 1 BOTTLE (51862-042-02) | 250 capsule | 2018-03-09 | 0000-00-00 | No | No | Current |
| 51862-042-05 | 51862004205 | 50 CAPSULE in 1 BOTTLE (51862-042-05) | 50 capsule | 2018-03-09 | 0000-00-00 | No | No | Current |