NDC 53489-647 – Doxycycline Hyclate
Doxycycline Hyclate 20 mg/1 · Tablet, Film Coated · Oral
Product NDC53489-647
Product details
- Brand name
- Doxycycline Hyclate
- Generic name
- Doxycycline Hyclate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA065134
- Marketed since
- May 13, 2005
- Listing expires
- December 31, 2026
- Pharmacologic class
- Tetracycline-class Drug
Active ingredients
- Doxycycline Hyclate 20 mg/1
Uses, dosage, side effects and warnings for Doxycycline Hyclate →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 53489-647-01 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-01) | May 13, 2005 |
| 53489-647-03 | 250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-03) | May 13, 2005 |
| 53489-647-05 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-05) | May 13, 2005 |
| 53489-647-06 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-06) | May 13, 2005 |
| 53489-647-07 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-07) | May 13, 2005 |
| 53489-647-10 | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-10) | May 13, 2005 |
| 53489-647-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-90) | May 13, 2005 |
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