Doxycycline Hyclate 53489-0120
Product NDC
53489-0120- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 10, 1986
- Listing Expires
- December 31, 2027
- Application
- ANDA062677
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Doxycycline Hyclate | 100 mg/1 |
Drug Class
Tetracycline-class Drug [EPC]Tetracyclines [CS]
Packaging Options(3)
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-120-01)
50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-120-02)
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-120-05)