66213-421 : Donnatal (Atropine Sulfate 0.0582 mg / Hyoscyamine Sulfate 0.311 mg / Phenobarbital 48.6 mg / Scopolamine Hydrobromide 0.0195 mg) Extended Release Tablet


NDC66213-421
Labeler: Pbm Pharmaceuticals, Inc
Product Type: Human Prescription Drug
Drug Name:  Donnatal Extentabs
Dosage Form: Oral Tablet, Film Coated, Extended Release
Rev. Date: 


Appearance:


Markings: P;421 OR 421
Shapes:  Round
Colors:  Green
Size (mm): 10
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.

P 421 OR 421: (66213-421) Donnatal (Atropine Sulfate 0.0582 mg / Hyoscyamine Sulfate 0.311 mg / Phenobarbital 48.6 mg / Scopolamine Hydrobromide 0.0195 mg) Extended Release Tablet by Pbm Pharmaceuticals, Inc
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:

  • 66213-421-10: 100 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (66213‑421‑10)
  • 66213-421-50: 500 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (66213‑421‑50)

Active Ingredients:

  • Atropine Sulfate
  • Hyoscyamine Sulfate
  • Phenobarbital
  • Scopolamine Hydrobromide

Dosage Strength:

  • .0582 mg
  • .3111 mg
  • 48.6 mg
  • .0195 mg

Inactive Ingredients:

  • Anhydrous Lactose
  • Calcium Sulfate, Unspecified
  • Silicon Dioxide
  • Calcium Phosphate, Dibasic, Anhydrous
  • Lactose Monohydrate
  • Magnesium Stearate
  • Stearic Acid
  • D&c Yellow No. 10
  • Fd&c Blue No. 1
  • Hypromellose 2208 (4000 Mpa.s)
  • Polydextrose
  • Polyethylene Glycol 2000
  • Titanium Dioxide
  • Triacetin

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 65084-450 Donnatal (Atropine Sulfate 0.0582 mg / Hyoscyamine Sulfate 0.311 mg / Phenobarbital 48.6 mg / Scopolamine Hydrobromide 0.0195 mg) Extended Release Tablet by Rxpak Division of Mckesson Corporation

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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.