Doxycycline Hyclate
- Product NDC
- 63629-7921
- 11-digit product format
- 636297921
- Labeler code
- 63629
- Product ID
- 63629-7921_e7e67fb7-91a0-46cc-8ce0-aa0acccb6baa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA065134
- Marketing category
- ANDA
- Marketing start
- 2005-05-13
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 20 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7921-1 | 63629792101 | 20 TABLET, FILM COATED in 1 BOTTLE (63629-7921-1) | 2019-02-18 | 0000-00-00 | No | No | Current |
| 63629-7921-2 | 63629792102 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-7921-2) | 2019-02-18 | 0000-00-00 | No | No | Current |
| 63629-7921-3 | 63629792103 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-7921-3) | 2019-02-18 | 0000-00-00 | No | No | Current |