Doxycycline
- Product NDC
- 63187-936
- 11-digit product format
- 631870936
- Labeler code
- 63187
- Product ID
- 63187-936_8c93d33f-1500-4f79-8841-caec0bcf121a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA204446
- Marketing category
- ANDA
- Marketing start
- 2016-04-29
- 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
- 2020-12-31
- 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 |
|---|
| 63187-936-14 | 63187093614 | 14 CAPSULE in 1 BOTTLE (63187-936-14) | 14 capsule | 2017-11-01 | 0000-00-00 | No | No | Current |
| 63187-936-20 | 63187093620 | 20 CAPSULE in 1 BOTTLE (63187-936-20) | 20 capsule | 2017-11-01 | 0000-00-00 | No | No | Current |
| 63187-936-30 | 63187093630 | 30 CAPSULE in 1 BOTTLE (63187-936-30) | 30 capsule | 2017-11-01 | 0000-00-00 | No | No | Current |