Doxycycline
- Product NDC
- 55700-323
- 11-digit product format
- 557000323
- Labeler code
- 55700
- Product ID
- 55700-323_1d9055b1-ce59-4d74-9d70-ee1c281480a7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- doxycycline
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| N12000U13O | DOXYCYCLINE | 17086-28-1 | DOXYCYCLINE |