Doxycycline Hyclate
- Product NDC
- 0378-4533
- 11-digit product format
- 003784533
- Labeler code
- 0378
- Product ID
- 0378-4533_be3e3742-cb93-4e54-9fe7-62fd2056f05f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- doxycycline hyclate
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- ANDA090431
- Marketing category
- ANDA
- Marketing start
- 2016-05-19
- Marketing end
- 2019-08-31
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 200 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