Doxycycline Hyclate 53489-0647
Product NDC
53489-0647- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 13, 2005
- Listing Expires
- December 31, 2026
- Application
- ANDA065134
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Doxycycline Hyclate | 20 mg/1 |
Drug Class
Tetracycline-class Drug [EPC]Tetracyclines [CS]
Packaging Options(7)
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-01)
250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-03)
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-05)
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-06)
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-07)
1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-10)
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-90)