51293-606 : Isoxsuprine Hydrochloride 10 mg Oral Tablet


NDC: 51293-606
Labeler: Eci Pharmaceuticals LLC
Product Type: Human Prescription Drug
Drug Name:  Isoxsuprine Hydrochloride
Dosage Form: Oral Tablet
Rev. Date: 


Appearance:


Markings: I10
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.

I10: (42582-100) Isoxsuprine Hydrochloride 10 mg Oral Tablet by Eci Pharmaceuticals LLC
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

  • 51293-606-01: 100 TABLET IN 1 BOTTLE (51293‑606‑01)
  • 51293-606-10: 1000 TABLET IN 1 BOTTLE (51293‑606‑10)

Active Ingredients:

  • Isoxsuprine Hydrochloride

Dosage Strength:

  • 10 mg

Inactive Ingredients:

  • Lactose Monohydrate
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Starch, Corn

Related Products:

Based on records with the same trade name.
  • 51293-605 Isoxsuprine Hydrochloride 20 mg Oral Tablet by Eci Pharmaceuticals LLC
  • 42582-100 Isoxsuprine Hydrochloride 10 mg Oral Tablet by Bi-coastal Pharmaceutical Corporation
  • 42582-101 Isoxsuprine Hydrochloride 10 mg Oral Tablet by Bi-coastal Pharma International Limited Liability Company
  • 42582-200 Isoxsuprine Hydrochloride 20 mg Oral Tablet by Bi-coastal Pharmaceutical Corporation
  • 42582-201 Isoxsuprine Hydrochloride 20 mg Oral Tablet by Bi-coastal Pharma International Limited Liability Company
  • 61971-065 Isoxsuprine Hydrochloride 20 mg Oral Tablet by Vista Pharmaceuticals, Inc.
  • 63549-919 Isoxsuprine Hydrochloride 20 mg Oral Tablet by Vedco Dba Valdar
  • 66576-101 Isoxsuprine Hydrochloride 10 mg Oral Tablet by Syntho Pharmaceuticals Inc.
  • 66576-201 Isoxsuprine Hydrochloride 10 mg Oral Tablet by Syntho Pharmaceuticals Inc.

NDC QR Code

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NDC 51293-606 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.