Doxycycline Hyclate
- Product NDC
- 60760-626
- 11-digit product format
- 607600626
- Labeler code
- 60760
- Product ID
- 60760-626_a8382b26-742d-15ea-e053-2995a90aba35
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA062505
- Marketing category
- ANDA
- Marketing start
- 2020-02-19
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 19XTS3T51U | DOXYCYCLINE HYCLATE | 24390-14-5 | DOXYCYCLINE HYCLATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-626-20 | 60760062620 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-626-20) | 2020-02-19 | 0000-00-00 | No | No | Current |
| 60760-626-60 | 60760062660 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-626-60) | 2020-06-10 | 0000-00-00 | No | No | Current |