Doxycycline Hyclate
- Product NDC
- 68788-8217
- 11-digit product format
- 687888217
- Labeler code
- 68788
- Product ID
- 68788-8217_bbeb86a9-acd5-4101-ae22-a30dfc2bb78d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc
- Application
- ANDA207773
- Marketing category
- ANDA
- Marketing start
- 2022-09-08
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE HYCLATE
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8217-1 | 68788821701 | 14 TABLET in 1 BOTTLE (68788-8217-1) | 14 tablet | 2022-09-08 | 0000-00-00 | No | No | Current |
| 68788-8217-2 | 68788821702 | 20 TABLET in 1 BOTTLE (68788-8217-2) | 20 tablet | 2022-09-08 | 0000-00-00 | No | No | Current |
| 68788-8217-3 | 68788821703 | 30 TABLET in 1 BOTTLE (68788-8217-3) | 30 tablet | 2022-09-08 | 0000-00-00 | No | No | Current |