16571-127 : Tolterodine Tartrate 2 mg Oral Tablet, Film Coated

NDC:	16571-127
Labeler:	Rising Pharma Holdings, Inc.
Product Type:	Human Prescription Drug
Drug Name:	Tolterodine Tartrate
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA204721
Rev. Date:	Jan 24, 2020

Appearance:

Markings:	P2
Shapes:	Round
Colors:	White
Size (mm):	6
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:

16571-127-01: 100 TABLET, FILM COATED IN 1 BOTTLE (16571‑127‑01)
16571-127-06: 60 TABLET, FILM COATED IN 1 BOTTLE (16571‑127‑06)
16571-127-50: 500 TABLET, FILM COATED IN 1 BOTTLE (16571‑127‑50)

Active Ingredients:

Tolterodine Tartrate

Dosage Strength:

2 mg

Inactive Ingredients:

Dibasic Calcium Phosphate Dihydrate
Microcrystalline Cellulose
Sodium Starch Glycolate Type a
Silicon Dioxide
Magnesium Stearate
Hypromellose, Unspecified
Stearic Acid
Titanium Dioxide /

Pharmaceutical Classes:

Cholinergic Muscarinic Antagonist [EPC]
Cholinergic Muscarinic Antagonists [MoA]

NDC QR Code

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NDC 16571-127 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.