Doxycycline
- Product NDC
- 63629-6637
- 11-digit product format
- 636296637
- Labeler code
- 63629
- Product ID
- 63629-6637_92789ae4-502a-4c5e-967e-c195c452ba1b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- doxycycline
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA065055
- Marketing category
- ANDA
- Marketing start
- 2000-12-01
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record