0093-4820 : Lorazepam 0.5 mg Oral Tablet

NDC:	0093-4820
Labeler:	Teva Pharmaceuticals USA Inc
Product Type:	Human Prescription Drug
Drug Name:	Lorazepam
Dosage Form:	Oral Tablet
Application #:	ANDA077396
Rev. Date:	Feb 1, 2007
CSA Schedule:	CIV (US) ^[1]

^[1] Schedule IV Controlled Substance: Low potential for abuse relative to substances in Schedule III. Examples include Alprazolam (Xanax), Diazepam (Valium), Carisoprodol (Soma), Clonazepam (Klonopin), Lorazepam (Ativan), Clorazepate (Tranxene), Midazolam (Versed), Temazepam (Restoril), and Triazolam (Halcion).. More Details: US Dept of Justice Controlled Substance Schedules.

Appearance:

Markings:	L
Shapes:	Round
Colors:	White
Size (mm):	5
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.

NDC Package Codes:

0093-4820-01: 100 TABLET IN 1 BOTTLE (0093‑4820‑01)
0093-4820-05: 500 TABLET IN 1 BOTTLE (0093‑4820‑05)
0093-4820-10: 1000 TABLET IN 1 BOTTLE (0093‑4820‑10)

Active Ingredients:

Lorazepam

Dosage Strength:

.5 mg

Inactive Ingredients:

Lactose Monohydrate
Magnesium Stearate
Cellulose, Microcrystalline
Hydroxypropyl Cellulose, Low Substituted

Pharmaceutical Classes:

Benzodiazepine [EPC]
Benzodiazepines [Chemical/Ingredient]

NDC 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.