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NDC 47781-0014-01 hyoscyamine sulfate 0.375 mg/1 Details
hyoscyamine sulfate 0.375 mg/1
hyoscyamine sulfate is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Alvogen Inc.. The primary component is HYOSCYAMINE SULFATE.
MedlinePlus Drug Summary
Hyoscyamine is used to control symptoms associated with disorders of the gastrointestinal (GI) tract. It works by decreasing the motion of the stomach and intestines and the secretion of stomach fluids, including acid. Hyoscyamine is also used in the treatment of bladder spasms, peptic ulcer disease, diverticulitis, colic, irritable bowel syndrome, cystitis, and pancreatitis. Hyoscyamine may also be used to treat certain heart conditions, to control the symptoms of Parkinson's disease and rhinitis (runny nose), and to reduce excess saliva production.
Related Packages: 47781-0014-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Hyoscyamine
Product Information
| NDC | 47781-0014 |
|---|---|
| Product ID | 47781-014_a62c7c6b-59e3-2426-d799-802d5b276ce9 |
| Associated GPIs | 49101030107420 |
| GCN Sequence Number | 023715 |
| GCN Sequence Number Description | hyoscyamine sulfate TAB ER 12H 0.375 MG ORAL |
| HIC3 | J2A |
| HIC3 Description | BELLADONNA ALKALOIDS |
| GCN | 18960 |
| HICL Sequence Number | 002017 |
| HICL Sequence Number Description | HYOSCYAMINE SULFATE |
| Brand/Generic | Generic |
| Proprietary Name | hyoscyamine sulfate |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | hyoscyamine sulfate |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, EXTENDED RELEASE |
| Route | ORAL |
| Active Ingredient Strength | 0.375 |
| Active Ingredient Units | mg/1 |
| Substance Name | HYOSCYAMINE SULFATE |
| Labeler Name | Alvogen Inc. |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Application Number | n/a |
| Listing Certified Through | 2024-12-31 |
Package
NDC 47781-0014-01 (47781001401)
| NDC Package Code | 47781-014-01 |
|---|---|
| Billing NDC | 47781001401 |
| Package | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47781-014-01) |
| Marketing Start Date | 2022-01-31 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |