Phenobarbital
- Product NDC
- 0463-6170
- 11-digit product format
- 004636170
- Labeler code
- 0463
- Product ID
- 0463-6170_ba250e94-ae3b-47ab-bf2e-cf7ea3a47d0a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenobarbital
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- C.O. Truxton, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2012-03-01
- Marketing end
- 0000-00-00
- Substance
- PHENOBARBITAL
- Active strength
- 100 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 0463-6170-01 | Phenobarbital | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
| 0463-6170-10 | Phenobarbital | 1000 in 1 BOTTLE | TABLET | 1000 | | 1 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| PHENOBARBITAL | ACTIVE INGREDIENT | YQE403BP4D | PHENOBARBITAL TABLET [C.O. TRUXTON, INC.] | 1 | |
| PHENOBARBITAL | ACTIVE MOIETY | YQE403BP4D | PHENOBARBITAL TABLET [C.O. TRUXTON, INC.] | 1 | |
| ANHYDROUS LACTOSE | INACTIVE INGREDIENT | 3SY5LH9PMK | PHENOBARBITAL TABLET [C.O. TRUXTON, INC.] | 1 | |
| CALCIUM STEARATE | INACTIVE INGREDIENT | 776XM7047L | PHENOBARBITAL TABLET [C.O. TRUXTON, INC.] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | PHENOBARBITAL TABLET [C.O. TRUXTON, INC.] | 1 | |
| DOCUSATE SODIUM | INACTIVE INGREDIENT | F05Q2T2JA0 | PHENOBARBITAL TABLET [C.O. TRUXTON, INC.] | 1 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | PHENOBARBITAL TABLET [C.O. TRUXTON, INC.] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | PHENOBARBITAL TABLET [C.O. TRUXTON, INC.] | 1 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | PHENOBARBITAL TABLET [C.O. TRUXTON, INC.] | 1 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | PHENOBARBITAL TABLET [C.O. TRUXTON, INC.] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | PHENOBARBITAL TABLET [C.O. TRUXTON, INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0463-6170 | PHENOBARBITAL TABLET [C.O. TRUXTON, INC.] | 1 | Legacy NDC, 2 package rows | 20121020_894c57ee-0f5f-41a1-9e0d-3f1f8fdfc9ab.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 0463-6170-01 | 00463617001 | 100 in 1 BOTTLE | Historical |
| 0463-6170-10 | 00463617010 | 1000 in 1 BOTTLE | Historical |