OXYBUTYNIN CHLORIDE
- Product NDC
- 66336-604
- 11-digit product format
- 663360604
- Labeler code
- 66336
- Product ID
- 66336-604_95753e38-0d1c-410c-9d1e-7e09dea1437c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXYBUTYNIN CHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Dispensing Solutions, Inc.
- Application
- ANDA076745
- Marketing category
- ANDA
- Marketing start
- 2007-05-11
- Marketing end
- 0000-00-00
- Substance
- OXYBUTYNIN CHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 66336-604-30 | OXYBUTYNIN CHLORIDE | 30 in 1 BOTTLE, PLASTIC | TABLET, EXTENDED RELEASE | 30 | | 1 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| OXYBUTYNIN CHLORIDE | ACTIVE INGREDIENT | L9F3D9RENQ | OXYBUTYNIN CHLORIDE TABLET, EXTENDED RELEASE [DISPENSING SOLUTIONS, INC.] | 1 | |
| OXYBUTYNIN | ACTIVE MOIETY | K9P6MC7092 | OXYBUTYNIN CHLORIDE TABLET, EXTENDED RELEASE [DISPENSING SOLUTIONS, INC.] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | OXYBUTYNIN CHLORIDE TABLET, EXTENDED RELEASE [DISPENSING SOLUTIONS, INC.] | 1 | |
| FD&C BLUE NO. 2 | INACTIVE INGREDIENT | L06K8R7DQK | OXYBUTYNIN CHLORIDE TABLET, EXTENDED RELEASE [DISPENSING SOLUTIONS, INC.] | 1 | |
| FD&C RED NO. 40 | INACTIVE INGREDIENT | WZB9127XOA | OXYBUTYNIN CHLORIDE TABLET, EXTENDED RELEASE [DISPENSING SOLUTIONS, INC.] | 1 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | OXYBUTYNIN CHLORIDE TABLET, EXTENDED RELEASE [DISPENSING SOLUTIONS, INC.] | 1 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | OXYBUTYNIN CHLORIDE TABLET, EXTENDED RELEASE [DISPENSING SOLUTIONS, INC.] | 1 | |
| METHACRYLIC ACID | INACTIVE INGREDIENT | 1CS02G8656 | OXYBUTYNIN CHLORIDE TABLET, EXTENDED RELEASE [DISPENSING SOLUTIONS, INC.] | 1 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | OXYBUTYNIN CHLORIDE TABLET, EXTENDED RELEASE [DISPENSING SOLUTIONS, INC.] | 1 | |
| TRIETHYL CITRATE | INACTIVE INGREDIENT | 8Z96QXD6UM | OXYBUTYNIN CHLORIDE TABLET, EXTENDED RELEASE [DISPENSING SOLUTIONS, INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66336-604 | OXYBUTYNIN CHLORIDE TABLET, EXTENDED RELEASE [DISPENSING SOLUTIONS, INC.] | 1 | Legacy NDC, 1 package rows | 20131030_d6e59c6b-4599-435e-b077-4f949bc8ed0a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 66336-604-30 | 66336060430 | 30 in 1 BOTTLE, PLASTIC | Historical |