Doxycycline Hyclate
- Product NDC
- 70625-208
- 11-digit product format
- 706250208
- Labeler code
- 70625
- Product ID
- 70625-208_dc67a4cf-8281-0a95-e053-2a95a90a9f56
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Praxgen Pharmaceuticals LLC
- Application
- ANDA212487
- Marketing category
- ANDA
- Marketing start
- 2022-09-01
- 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 |
|---|
| 70625-208-01 | 70625020801 | 50 TABLET, FILM COATED in 1 BOTTLE (70625-208-01) | 2022-09-15 | 0000-00-00 | No | No | Current |
| 70625-208-02 | 70625020802 | 500 TABLET, FILM COATED in 1 BOTTLE (70625-208-02) | 2022-09-15 | 0000-00-00 | No | No | Current |