69102-319 : Subvenite 100 mg Oral Tablet


NDC69102-319
Labeler: Owp Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Drug Name:  Subvenite
Dosage Form: Oral Tablet
Application #: ANDA078947
Rev. Date: 


Appearance:


Markings: 10LA
Shapes:  Round
Colors:  White
Size (mm): 9
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:

  • 69102-319-01: 100 TABLET IN 1 BOTTLE (69102‑319‑01)
  • 69102-319-02: 2500 TABLET IN 1 BOTTLE (69102‑319‑02)

Active Ingredients:

  • Lamotrigine

Dosage Strength:

  • 100 mg

Inactive Ingredients:

  • Lactose Monohydrate
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Povidone K30
  • Sodium Starch Glycolate Type a Potato /

Pharmaceutical Classes:

  • Decreased Central Nervous System Disorganized Electrical Activity [PE]
  • Mood Stabilizer [EPC]
  • Anti-epileptic Agent [EPC]

Related Products:

Based on records with the same trade name.
  • 69102-025 Subvenite 25 mg Oral Tablet by Owp Pharmaceuticals, Inc.
  • 69102-150 Subvenite 150 mg Oral Tablet by Owp Pharmaceuticals, Inc.
  • 69102-300 Subvenite Kit by Owp Pharmaceuticals, Inc.
  • 69102-301 Subvenite 25 mg Oral Tablet by Owp Pharmaceuticals, Inc.
  • 69102-306 Subvenite Kit by Owp Pharmaceuticals, Inc.
  • 69102-312 Subvenite Kit by Owp Pharmaceuticals, Inc.
  • 69102-320 Subvenite 200 mg Oral Tablet by Owp Pharmaceuticals, Inc.
  • 70518-2645 Subvenite 200 mg Oral Tablet by Remedyrepack Inc.

NDC QR Code

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NDC 69102-319 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.