Doxycycline
- Product NDC
- 42291-156
- 11-digit product format
- 422910156
- Labeler code
- 42291
- Product ID
- 42291-156_d57994f7-b649-7573-e053-2a95a90a9b76
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA065285
- Marketing category
- ANDA
- Marketing start
- 2019-02-15
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-156-05 | 42291015605 | 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42291-156-05) | 2019-02-15 | 0000-00-00 | No | No | Current |
| 42291-156-25 | 42291015625 | 250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42291-156-25) | 2019-02-15 | 0000-00-00 | No | No | Current |