Theophylline
- Product NDC
- 29033-001
- 11-digit product format
- 290330001
- Labeler code
- 29033
- Product ID
- 29033-001_cc6d208a-826c-4aae-a78e-da1a91c60699
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Theophylline
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Nostrum Laboratories, Inc.
- Application
- ANDA040560
- Marketing category
- ANDA
- Marketing start
- 2020-01-23
- Marketing end
- 0000-00-00
- Substance
- THEOPHYLLINE ANHYDROUS
- Active strength
- 400 mg/1
- Pharmacologic classes
- Methylxanthine [EPC],Xanthines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 29033-001-01 | Theophylline(Anhydrous) | 100 in 1 BOTTLE, PLASTIC | TABLET, EXTENDED RELEASE | 100 | | 6 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 29033-001 | THEOPHYLLINE (ANHYDROUS) (THEOPHYLLINE) TABLET, EXTENDED RELEASE [NOSTRUM LABORATORIES, INC.] | 6 | Legacy NDC, 1 package rows | 20211103_038c2b07-8028-4dc4-847c-adafe1b0e81a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 29033-001-01 | 29033000101 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29033-001-01) | 2020-01-23 | 0000-00-00 | No | No | Current |