Doxycycline Hyclate
- Product NDC
- 70934-951
- 11-digit product format
- 709340951
- Labeler code
- 70934
- Product ID
- 70934-951_d79d34e8-adc1-fc11-e053-2a95a90a66d2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA062676
- Marketing category
- ANDA
- Marketing start
- 2022-02-09
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 50 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
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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-951-30 | 70934095130 | 30 CAPSULE in 1 BOTTLE, PLASTIC (70934-951-30) | 30 capsule | 2022-02-09 | 0000-00-00 | No | No | Current |