49999-039 : Alprazolam 0.25 mg Oral Tablet

NDC:	49999-039
Labeler:	Lake Erie Medical Dba Quality Care Products LLC
Product Type:	Human Prescription Drug
Drug Name:	Alprazolam
Dosage Form:	Oral Tablet
Application #:	ANDA074112
Rev. Date:	Apr 1, 2010
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:	GG256
Shapes:	Oval
Colors:	White
Size (mm):	25
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:

49999-039-10: 10 TABLET IN 1 BOTTLE, PLASTIC (49999‑039‑10)
49999-039-15: 15 TABLET IN 1 BOTTLE, PLASTIC (49999‑039‑15)
49999-039-30: 30 TABLET IN 1 BOTTLE, PLASTIC (49999‑039‑30)
49999-039-60: 60 TABLET IN 1 BOTTLE, PLASTIC (49999‑039‑60)
49999-039-90: 90 TABLET IN 1 BOTTLE, PLASTIC (49999‑039‑90)

Active Ingredients:

Alprazolam

Dosage Strength:

.25 mg

Inactive Ingredients:

Lactose Monohydrate
Docusate Sodium
Cellulose, Microcrystalline
Magnesium Stearate
Starch, Corn
Sodium Benzoate

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.