Doxycycline
- Product NDC
- 63629-7970
- 11-digit product format
- 636297970
- Labeler code
- 63629
- Product ID
- 63629-7970_11a1b73c-fe08-40f2-b5e6-548748a328e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204446
- Marketing category
- ANDA
- Marketing start
- 2015-05-28
- Marketing end
- 2022-10-31
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| N12000U13O | DOXYCYCLINE | 17086-28-1 | DOXYCYCLINE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7970-1 | 63629797001 | 20 CAPSULE in 1 BOTTLE (63629-7970-1) | 20 capsule | 2019-03-13 | 2022-10-31 | No | No | Current |