Prescription drug · UNAPPROVED DRUG OTHER
Hyoscyamine Sulfate SL (hyoscyamine sulfate) NDC 71335-1159
Hyoscyamine sulfate .125 mg/1 · Tablet · Sublingual · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71335-1159-0 | 71335115900 | 10 TABLET in 1 BOTTLE (71335-1159-0)Marketed from Oct 31, 2024 | |
| 71335-1159-1 | 71335115901 | 20 TABLET in 1 BOTTLE (71335-1159-1)Marketed from Apr 20, 2020 | |
| 71335-1159-2 | 71335115902 | 30 TABLET in 1 BOTTLE (71335-1159-2)Marketed from Mar 19, 2019 | |
| 71335-1159-3 | 71335115903 | 15 TABLET in 1 BOTTLE (71335-1159-3)Marketed from Oct 31, 2024 | |
| 71335-1159-4 | 71335115904 | 21 TABLET in 1 BOTTLE (71335-1159-4)Marketed from Oct 31, 2024 | |
| 71335-1159-5 | 71335115905 | 60 TABLET in 1 BOTTLE (71335-1159-5)Marketed from Oct 31, 2024 | |
| 71335-1159-6 | 71335115906 | 12 TABLET in 1 BOTTLE (71335-1159-6)Marketed from Aug 2, 2024 | |
| 71335-1159-7 | 71335115907 | 90 TABLET in 1 BOTTLE (71335-1159-7)Marketed from Dec 13, 2021 | |
| 71335-1159-8 | 71335115908 | 100 TABLET in 1 BOTTLE (71335-1159-8)Marketed from Jan 4, 2022 | |
| 71335-1159-9 | 71335115909 | 45 TABLET in 1 BOTTLE (71335-1159-9)Marketed from Oct 31, 2024 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Hyoscyamine Sulfate SL
- Generic name (nonproprietary)
- hyoscyamine sulfate
- Active ingredients
- Hyoscyamine sulfate — .125 mg/1
- Dosage form
- Tablet
- Route
- Sublingual
- Labeler
- Bryant Ranch Prepack
- Product type
- Prescription drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- Identifiers
- Product ID 71335-1159_b47f4839-f717-4afa-be2c-f33f6b5c71a3SPL ID b47f4839-f717-4afa-be2c-f33f6b5c71a3SPL set ID 3749da41-19f3-46b2-887d-7f8ae2268700RxCUI 1046982UNII F2R8V82B84
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N471335115900followed by a unit qualifier and the quantityPackage 71335-1159-00. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
INDICATIONS AND USAGE This product may be used in functional intestinal disorders to reduce symptoms such as those seen in mild dysenteries and diverticulitis. It can also be used to control gastric secretion, visceral spasm and hypermotility in cystitis, pylorospasm and associated abdominal cramps. Along with appropriate analgesics, this product is indicated in symptomatic relief of biliary and renal colic and as a drying agent in the relief of symptoms of acute rhinitis. This product is effective as adjunctive therapy in the treatment of peptic ulcer and irritable bowel syndrome, acute enterocolitis and other functional gastrointestinal disorders.
Excerpt only. Read the full label for complete information.