Doxycycline
- Product NDC
- 60760-215
- 11-digit product format
- 607600215
- Labeler code
- 60760
- Product ID
- 60760-215_f06e8d19-c6ea-6cba-e053-2995a90a3adb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline hyclate
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- St Marys Medical Park Pharmacy
- Application
- ANDA065095
- Marketing category
- ANDA
- Marketing start
- 2003-07-02
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC], Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 60760-215-20 | 60760021520 | 20 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-215-20) | 2010-12-01 | 0000-00-00 | No | No | Current |
| 60760-215-60 | 60760021560 | 60 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-215-60) | 2003-07-02 | 0000-00-00 | No | No | Current |