0093-0318 : Diltiazem Hydrochloride 30 mg Oral Tablet

NDC:	0093-0318
Labeler:	Teva Pharmaceuticals USA Inc
Product Type:	Human Prescription Drug
Drug Name:	Diltiazem Hydrochloride
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA074185
Rev. Date:	Dec 22, 1995

Appearance:

Markings:	93;318
Shapes:	Round
Colors:	Orange
Size (mm):	8
Segments: ^*	1
^* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

93 318: (0093-0318) Diltiazem Hydrochloride 30 mg Oral Tablet by Teva Pharmaceuticals USA Inc

The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

0093-0318-01: 100 TABLET, FILM COATED IN 1 BOTTLE (0093‑0318‑01)
0093-0318-05: 500 TABLET, FILM COATED IN 1 BOTTLE (0093‑0318‑05)

Active Ingredients:

Diltiazem Hydrochloride

Dosage Strength:

30 mg

Inactive Ingredients:

Hypromelloses
Lactose Monohydrate
Magnesium Stearate
Polyethylene Glycols
Polysorbate 80
Povidone
Titanium Dioxide
Fd&c Yellow No. 6
Aluminum Oxide

Pharmaceutical Classes:

Calcium Channel Antagonists [MoA]
Calcium Channel Blocker [EPC]

NDC QR Code

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NDC 0093-0318 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.