Doxycycline Hyclate
- Product NDC
- 69597-345
- 11-digit product format
- 695970345
- Labeler code
- 69597
- Product ID
- 69597-345_fe3b62b7-8b91-4de8-a2e9-9eb41a76a05d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Basiem
- Application
- NDA050795
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-04-04
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 80 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