66336-871 : Homatropine Methylbromide 1.5 mg / Hydrocodone Bitartrate 5 mg Oral Tablet

NDC:	66336-871
Labeler:	Dispensing Solutions, Inc.
Product Type:	Human Prescription Drug
Drug Name:	Hydrocodone Bitartrate and Homatropine Methylbromide
Dosage Form:	Oral Tablet
Application #:	ANDA091528
Rev. Date:	Feb 16, 2011
CSA Schedule:	CIII (US) [1]

^[1] Schedule III / IIIN Controlled Substance: Has a potential for abuse less than substances in Schedules I or II and abuse may lead to moderate or low physical dependence or high psychological dependence. (i.e. Products containing not more than 90 milligrams of Codeine per dosage unit [such as Tylenol with Codeine], other narcotics such as Buprenorphine (Suboxone), and Schedule IIIN non-narcotics such as Didrex, Ketamine, Phendimetrazine, and Anabolic Steroids). More Details: US Dept of Justice Controlled Substance Schedules.

Appearance:

Markings:	N;350
Shapes:	Round
Colors:	White
Size (mm):	8
Segments: *	2
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces.

NDC Package Codes:

• 66336-871-15: 15 TABLET IN 1 BOTTLE (66336‑871‑15)

Active Ingredients:

• Homatropine Methylbromide
• Hydrocodone Bitartrate

Inactive Ingredients:

• Anhydrous Lactose
• Anhydrous Dibasic Calcium Phosphate
• Sodium Starch Glycolate Type a Potato
• Silicon Dioxide
• Magnesium Stearate

Pharmaceutical Classes:

• Opioid Agonist [EPC]
• Opioid Agonists [MoA]

Related Products:

Based on records with the same trade name.

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• 60687-278 Hydrocodone Bitartrate and Homatropine Methylbromide Oral Syrup by American Health Packaging
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• More related products ...

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