Doxycycline
- Product NDC
- 43063-886
- 11-digit product format
- 430630886
- Labeler code
- 43063
- Product ID
- 43063-886_cfd4f252-f547-7650-e053-2a95a90ae32b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA204446
- Marketing category
- ANDA
- Marketing start
- 2015-05-28
- 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 |
|---|
| 43063-886-20 | 43063088620 | 20 CAPSULE in 1 BOTTLE, PLASTIC (43063-886-20) | 20 capsule | 2018-08-17 | 0000-00-00 | No | No | Current |
| 43063-886-60 | 43063088660 | 60 CAPSULE in 1 BOTTLE, PLASTIC (43063-886-60) | 60 capsule | 2018-08-17 | 0000-00-00 | No | No | Current |