10135-590 : Pilocarpine Hydrochloride 7.5 mg Oral Tablet, Film Coated
NDC: | 10135-590 |
Labeler: | Marlex Pharmaceuticals Inc |
Product Type: | Human Prescription Drug |
Drug Name: | Pilocarpine Hydrochloride |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA077220 |
Rev. Date: |
Appearance:
Markings: | LCI;1407 |
Shapes: |
Round |
Colors: |
Blue |
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. |
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:
- 10135-590-01: 100 TABLET, FILM COATED IN 1 BOTTLE (10135‑590‑01)
Active Ingredients:
- Pilocarpine Hydrochloride
Dosage Strength:
- 7.5 mg
Inactive Ingredients:
- Cellulose, Microcrystalline
- Stearic Acid
- Fd&c Blue No. 2
- Indigotindisulfonate Sodium
- Polyvinyl Alcohol
- Titanium Dioxide
- Polyethylene Glycols
- Talc
Pharmaceutical Classes:
- Cholinergic Agonists [MoA]
- Cholinergic Muscarinic Agonists [MoA]
- Cholinergic Receptor Agonist [EPC]
Related Products:
Based on records with the same trade name.- 10135-589 Pilocarpine Hydrochloride 5 mg Oral Tablet, Film Coated by Marlex Pharmaceuticals Inc
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- 17478-223 Pilocarpine Hydrochloride 10 mg/ml Ophthalmic Solution/ Drops by Akorn, Inc.
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- 52125-502 Pilocarpine Hydrochloride 40 mg/1 Ophthalmic Solution by Remedyrepack Inc.
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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.