NDC 53489-676 – Phentermine Hydrochloride
Phentermine Hydrochloride 37.5 mg/1 · Tablet · Oral
Product NDC53489-676
Product details
- Brand name
- Phentermine Hydrochloride
- Generic name
- Phentermine Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA040526
- Marketed since
- August 12, 2013
- Listing expires
- December 31, 2026
- Pharmacologic class
- Sympathomimetic Amine Anorectic
Active ingredients
- Phentermine Hydrochloride 37.5 mg/1
Uses, dosage, side effects and warnings for Phentermine Hydrochloride →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 53489-676-01 | 100 TABLET in 1 BOTTLE, PLASTIC (53489-676-01) | Aug 12, 2013 |
| 53489-676-03 | 250 TABLET in 1 BOTTLE, PLASTIC (53489-676-03) | Aug 12, 2013 |
| 53489-676-05 | 500 TABLET in 1 BOTTLE, PLASTIC (53489-676-05) | Aug 12, 2013 |
| 53489-676-06 | 60 TABLET in 1 BOTTLE, PLASTIC (53489-676-06) | Aug 12, 2013 |
| 53489-676-07 | 30 TABLET in 1 BOTTLE, PLASTIC (53489-676-07) | Aug 12, 2013 |
| 53489-676-10 | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-676-10) | Aug 12, 2013 |
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