Doxycycline 63304-0130
Product NDC
63304-0130- Manufacturer
- Sun Pharmaceutical Industries Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 6, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA065356
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Doxycycline | 50 mg/1 |
Drug Class
Tetracycline-class Drug [EPC]Tetracycline-class Drug [EPC]Tetracyclines [CS]
Packaging Options(1)
1000 TABLET, FILM COATED in 1 BOTTLE (63304-130-10)