Acticlate
- Product NDC
- 16110-502
- 11-digit product format
- 161100502
- Labeler code
- 16110
- Product ID
- 16110-502_6655b5f0-f3b7-11eb-85b4-0800200c9a66
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- doxycycline hyclate
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Almirall, LLC
- Application
- NDA205931
- Marketing category
- NDA
- Marketing start
- 2014-07-28
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 150 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16110-502-01 | 16110050201 | 60 TABLET, COATED in 1 BOTTLE (16110-502-01) | 2014-07-28 | 0000-00-00 | No | No | Current |