NDC 53489-676 – Phentermine Hydrochloride

Phentermine Hydrochloride 37.5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

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

Uses, dosage, side effects and warnings for Phentermine Hydrochloride →

Package NDC codes (6)

Package NDCDescriptionSince
53489-676-01100 TABLET in 1 BOTTLE, PLASTIC (53489-676-01)Aug 12, 2013
53489-676-03250 TABLET in 1 BOTTLE, PLASTIC (53489-676-03)Aug 12, 2013
53489-676-05500 TABLET in 1 BOTTLE, PLASTIC (53489-676-05)Aug 12, 2013
53489-676-0660 TABLET in 1 BOTTLE, PLASTIC (53489-676-06)Aug 12, 2013
53489-676-0730 TABLET in 1 BOTTLE, PLASTIC (53489-676-07)Aug 12, 2013
53489-676-101000 TABLET in 1 BOTTLE, PLASTIC (53489-676-10)Aug 12, 2013

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