Doxycycline Hyclate
- Product NDC
- 0591-6125
- 11-digit product format
- 005916125
- Labeler code
- 0591
- Product ID
- 0591-6125_df7ec0d5-8def-40cd-b5df-c257ed029c8e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Actavis Pharma, Inc.
- Application
- NDA205931
- Marketing category
- NDA
- Marketing start
- 2017-06-19
- 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 |
|---|
| 0591-6125-60 | 00591612560 | 60 TABLET, FILM COATED in 1 BOTTLE (0591-6125-60) | 2017-06-19 | 0000-00-00 | No | No | Current |