Doxycycline
- Product NDC
- 68084-743
- 11-digit product format
- 680840743
- Labeler code
- 68084
- Product ID
- 68084-743_ea3f954e-22ca-0c7a-e053-2995a90a7cd1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA065055
- Marketing category
- ANDA
- Marketing start
- 2014-05-13
- Marketing end
- 2024-12-31
- Substance
- DOXYCYCLINE
- Active strength
- 100 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 |
|---|
| 68084-743-21 | 68084074321 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-743-21) > 1 CAPSULE in 1 BLISTER PACK (68084-743-11) | 30 blister pack | 2020-01-20 | 0000-00-00 | No | No | Current |
| 68084-743-32 | 68084074332 | 20 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-743-32) > 1 CAPSULE in 1 BLISTER PACK (68084-743-33) | 20 blister pack | 2014-05-13 | 0000-00-00 | No | No | Current |